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SINthetic Pharmaceutical = ‘Poison of the Witch’ The Word Pharmacy is from the Greek ‘The Poison of a Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’ When a large percentage of the drugs once approved for sale need to be removed for hurting people, We must see that there is something extremely wrong with the Approval process. What is wrong is that SINthetic Patented PHARMACeuticals are trully the ‘Poison of the Witch’.

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SINthetic Pharmaceutical = ‘Poison of the Witch’ This Book will list some of these removed drugs and explain the danger.

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’

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SINthetic Pharmaceutical = ‘Poison of the Witch’ This is a list of the Major drugs once approved for use now recalled a dangerous

Australia, France, Oxyphenisatin (Phenisatin) Hepatotoxicity.[3] Germany, UK, US

[3] Secobarbital France, Norway, others. Self poisoning.

Marketed as a psychiatric 1950 drug; withdrawn after it Lysergic acid s– became widely used diethylamide (LSD) 1960 recreationally. Now illegal in s most of the world.

[3][53] Thenalidine 1960 Canada, UK, US Neutropenia

Withdrawn because of risk of teratogenicity;[52] returned to market for use

Thalidomide 1961 Germany in leprosy and multiple myeloma under FDAorphan drug rules

Cataracts, alopecia,

Triparanol 1962 France, US ichthyosis.[3]

[9] Bunamiodyl 1963 Canada, UK, US Nephropathy.

Genotoxicity.[13] withdrawn

Dantron 1963 Canada, UK, US from general use in UK but permitted in terminal patients

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SINthetic Pharmaceutical = ‘Poison of the Witch’

[20] Ethyl carbamate 1963 Canada, UK, US, Carcinogenicity.

[3] Benziodarone 1964 France, UK Jaundice.

Butamben (Efocaine)(Butoform Dermatologic toxicity; 1964 US e) psychiatric Reactions.[3]

Cardiovascular and

Dithiazanine iodide 1964 France, US metabolic reaction.[3]

[3] Iodinated casein strophantin 1964 US Metabolic reaction.

Interactions with food

Iproniazid 1964 Canada products containing .[22]

Unspecific experimental

Metofoline 1965 US toxicity.[3]

[3] 1965 UK Animal carcinogenicity.

[3] Xenazoic acid 1965 France Hepatotoxicity.

Hepatotoxicity, drug

Phenoxypropazine 1966 UK intereaction.[3]

[3] Bithionol 1967 US Dermatologic toxicity.

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SINthetic Pharmaceutical = ‘Poison of the Witch’

[3] Ibufenac 1968 UK Hepatotoxicity, jaundice.

[3] Anagestone acetate 1969 Germany Animal carcinogenicity.

[3] 1969 Germany Cardiovascular Toxicity.

[3] Cloforex 1969 Germany Cardiovascular toxicity.

Dermatologic and ophthalmic

Amoproxan 1970 France toxicity.[3]

Chlormadinone(Chlormenadion 1970 UK, US Animal Carcinogenicity.[3] e)

1970 Risk of teratogenicity[citation

Diethylstilbestrol s needed]

[3] Dihydrostreptomycin 1970 US Neuropsychiatric reaction.

Jaundice, elevated hepatic

Fenclozic acid 1970 UK, US enzymes.[3]

[3] Diacetoxydiphenolisatin 1971 Australia Hepatotoxicity.

[3] Triacetyldiphenolisatin 1971 Australia Hepatotoxicity.

Dimazole (Diamthazole) 1972 France, US Neuropsychiatric reaction.[3]

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SINthetic Pharmaceutical = ‘Poison of the Witch’

France, Germany, UK, [3] Clioquinol 1973 Neurotoxicity. US

Hepatotoxicity, drug

Nialamide 1974 UK, US intereaction.[3]

Agranulocytosis, Dipyrone(Metamizole) 1975 UK, US, Others anaphylactic reactions.[3]

Hepatotoxicity, drug

Mebanazine 1975 UK intereaction.[3]

An ingredient in "A.P.C." tablet; withdrawn because of risk of cancer and kidney

Phenacetin 1975 Canada disease[32] Germany Denmark, UK, US, others Reason: nephropathy.[3]

[3] Azaribine 1976 US Thromboembolism.

[29] Oxeladin 1976 Canada, UK, US (1976) Carcinogenicity.

Pifoxime (=Pixifenide) 1976 France Neuropsychiatric reaction.[3]

Phenformin and Buformin 1977 France, Germany US Severe lactic acidosis[3]

[3] Buformin 1978 Germany Metabolic toxicity.

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SINthetic Pharmaceutical = ‘Poison of the Witch’

[3] Alclofenac 1979 UK Vasculitis, Rash.

[3] Methapyrilene 1979 Germany, UK, US Animal carcinogenicity.

[3] 1979 France Abuse.

[3] Amobarbital 1980 Norway Self poisoning.

[3] Cyclobarbital 1980 Norway Self poisoning.

[3] Pentobarbital 1980 Norway Self poisoning.

Germany, France, UK, Ticrynafen(Tienilic acid) 1980 Liver toxicity and death.[3] US others

1981 Hemolytic Anemia, France, Germany, Spain,

Nomifensine - hepatotoxicity, serious UK, US, others 1986 hypersensitive reactions.[2][3]

Liver and kidney failure;

Benoxaprofen 1982 Germany,Spain, UK, US gastrointestinal bleeding; ulcers.[2][3]

[3] Clomacron 1982 UK Hepatotoxicity.

France, Germany, UK, [3] Methandrostenolone 1982 Off-label abuse. US, others

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SINthetic Pharmaceutical = ‘Poison of the Witch’

Withdrawn for inability to produce effective convulsive

Pentylenetetrazol 1982 therapy, and for causing seizures.

Voluntarily withdrawn from market by Lily.[15]:12Reintroduced as a dietary supplement in Dimethylamylamine (DMAA) 1983 US 2006;[15]:13 and in 2013 the FDA started work to ban it due to cardiovascular problems[16]

Animal carcinogenicity,

Indoprofen 1983 Germany, Spain, UK gastrointestinal toxicity.[3]

France, Germany, Spain, [3] Isoxicam 1983 Stevens johnson syndrome. others

[3] Propanidid 1983 UK Allergy.

Risk of Guillain-Barré syndrome, hypersensitivity

Zimelidine 1983 Worldwide reaction, hepatotoxicity[3][57][58] banned worldwide.[59]

Anaphylactic reactions and

Zomepirac 1983 UK, Germany, Spain, US non-fatal allergic reactions, renal failure[2][3]

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SINthetic Pharmaceutical = ‘Poison of the Witch’

Althesin (=Alphaxoloneaminept 1984 France, Germany, UK Anaphylaxis.[3] ine + Alphadolone)

Unspecific experimental

Antrafenine 1984 France toxicity.[3]

Cutaneous reactions; animal

Fenclofenac 1984 UK carcinogenicity.[3]

Cutaneous reaction,

Feprazone 1984 Germany, UK multiorgan toxicity.[3]

[3] Glafenine 1984 France, Germany Anaphylaxis.

[3] Isaxonine phosphate 1984 France Hepatotoxicity.

South Africa (1971), India Withdrawn because of risk

[26][2 Methaqualone 1984 (1984), United Nations of addiction and overdose (1971-1988) 7]

Hepatic and hematologic

Nitrefazole 1984 Germany toxicity.[3]

1984 Bone marrow suppression, UK, US, Germany,

Oxyphenbutazone - Steven Johnson France, Canada 1985 Syndrome.[3][30]

France, Germany, Spain, [3] Cianidanol 1985 Hemolytic Anemia. Sweden

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SINthetic Pharmaceutical = ‘Poison of the Witch’

[3] Indalpine 1985 France Agranulocytosis.

Neurologic and hepatic

Perhexilene 1985 UK, Spain toxicity.[3]

Off-label abuse, hematologic

Phenylbutazone 1985 Germany toxicity.[3]

[3] Suloctidyl 1985 Germany, France, Spain Hepatotoxicity.

Renal toxicity, animal

Beta-ethoxy-lacetanilanide 1986 Germany carcinogenicity.[3]

[3] Bucetin 1986 Germany Renal toxicity.

[3] Canrenone 1986 Germany Animal Carcinogenicity.

[3] Difemerine 1986 Germany Multi-Organ toxicities.

Dermatologic and

Sulfamethoxypyridazine 1986 UK hematologic reactions.[3]

1986 Flank pain, decreased kidney

Suprofen - UK, Spain, US function.[2][3] 1987

[3] Clometacin 1987 France Hepatotoxicity.

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SINthetic Pharmaceutical = ‘Poison of the Witch’

[3] Cyclofenil 1987 France Hepatotoxicity.

France,

[3] Muzolimine 1987 Germany,European Polyneuropathy. Union

[3] Vincamine 1987 Germany Hematologic toxicity.

[10][11] Cinepazide 1988 Spain Agranulocytosis.

[3] Nikethamide 1988 multiple markets CNS Stimulation.

Canada,France, Cardiac arrythmia[37] and

Prenylamine 1988 Germany, UK, US, others death.[3]

Dermatologic, hematologic

Sulfacarbamide 1988 Germany and hepatic reactions .[3]

[3] Sulfamethoxydiazine 1988 Germany Unknown.

[3] Broazolam 1989 UK Animal carcinogenicity.

Withdrawn US (1999). Risk

Etretinate 1989 France for birth defects.[2][3]

[3] Exifone 1989 France Hepatotoxicity.

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SINthetic Pharmaceutical = ‘Poison of the Witch’

Eosinophilic myalgia

[3] L- 1989 Germany, UK syndrome. Still sold in the US

[3] Proglumide 1989 Germany Respiratory reaction.

[3] Dilevalol 1990 UK Hepatotoxicity.

Uterine hypotonus, fetal

Dinoprostone 1990 UK distress.[3]

[3] Fenoterol 1990 New Zealand Asthma mortality.

[3] Metipranolol 1990 UK, others Uveitis.

[3][36]:223 Pirprofen 1990 France, Germany, Spain Liver toxicity.

[2][3] Encainide 1991 UK, US Ventricular arrhythmias.

[3] Fipexide 1991 France Hepatotoxicity.

[3] Flunitrazepam 1991 France Abuse.

Prolonged QT interval, Germany, UK, Spain, Terodiline (Micturin) 1991 ventricular tachycardia and others arrhythmia.[3]

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SINthetic Pharmaceutical = ‘Poison of the Witch’

France, Netherlands, Psychiatric adverse drug

Triazolam 1991 Finland, Argentina, UK reactions, amnesia.[3][56] others

[3] Benzarone 1992 Germany Hepatitis.

Low blood sugar; hemolytic anemia; kidney, liver

Temafloxacin 1992 Germany, UK, US, others dysfunction; allergic reactions[2][3]

Allergic reactions and cases

Temafloxacin 1992 US of hemolytic anemia, leading to three patient deaths.[2]

[3] Bendazac 1993 Spain Hepatotoxicity.

Increased mortality at higher Flosequinan (Manoplax) 1993 UK, US doses; increased hospitalizations.[2][3]

[3] Ketorolac 1993 France, Germany, others Hemorrhage, renal Failure.

[3] Moxisylyte 1993 France Necrotic hepatitis.

[3] Remoxipride 1993 UK, others Aplastic anemia.

Drug interaction and

Sorivudine 1993 Japan deaths.[50]

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SINthetic Pharmaceutical = ‘Poison of the Witch’

[3] Thiobutabarbitone 1993 Germany Renal insufficiency.

Not approved in the US, withdrawn in France in 1994[4]and the rest of the Alpidem (Ananxyl) 1995 Worldwide market in 1995 because of rare but serious hepatotoxicity.[3][5]

Hepatotoxicity; Steven- European Union, US, Chlormezanone (Trancopal) 1996 Johnson Syndrome; Toxic South Africa, Japan Epidermal Necrolysis.[3]

[3] Minaprine 1996 France Convulsions.

Argentina, Canada, Italy, Tolrestat (Alredase) 1996 Severe hepatotoxicity[3] others

[3] 1997 European Union, UK, US Cardiac valvular disease.

Fen-phen (popular combination of and phentermin 1997 Cardiotoxicity e)

European Union, UK, US, Cardiac valvular disease,

Fenfluramine 1997 India, South Africa, pulmonary hypertension, others cardiac fibrosis.[3][21]

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SINthetic Pharmaceutical = ‘Poison of the Witch’

Withdrawn from US in 2005. (Cylert) 1997 Canada, UK Hepatotoxicity[31]Reason:hep atotoxicity.[3]

[33] Phenolphthalein 1997 US Carcinogenicity.

1997 Terfenadine (Seldane, France, South Africa, Prolonged QT interval; - Triludan) Oman, others, US ventricular tachycardia[2][3] 1998

Severe hepatitis and liver

Bromfenac 1998 US failure (some requiring transplantation).[2]

[3] Ebrotidine 1998 Spain Hepatotoxicity.

European Union, Fatal arrhythmia, drug

Mibefradil 1998 Malaysia, US, others interactions.[2][3]

Spain, France, Italy, Immunoallergic,

Proxibarbal 1998 Portugal, Turkey thrombocytopenia.[3]

Arrhythmia and sudden

Sertindole 1998 European Union cardiac death[3][38]

European Union, Tolcapone (Tasmar) 1998 Hepatotoxicity[3] Canada, Australia

Amineptine (Survector) 1999 France, US Hepatotoxicity, dermatologic al side effects,

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SINthetic Pharmaceutical = ‘Poison of the Witch’

and abusepotential.[6] Reaso n:

risk of agranulocytosis;

Aminopyrine 1999 France, Thailand severe acne.[3]

US, Malaysia, Multiple Astemizole (Hismanal) 1999 Fatal arrhythmia[2][3] Nonspecified Markets

Withdrawn Germany, UK, Cardiac repolarization; QT Grepafloxacin (Raxar) 1999 US others interval prolongation.[2]

Still used as veterinary drug and as a human antihelminthic in many markets; listed on the WHO Levamisole (Ergamisol) 1999 US List of Essential Medicines. In humans, it was used to treat melanoma before it was withdrawn for agranulocytosis.[23][24][25]

Diversion, abuse, and a relatively high rate of overdose deaths in Temazepam (Restoril, comparison to other drugs of Euhypnos, Normison, 1999 Sweden, Norway its group. This drug Remestan, Tenox, Norkotral) continues to be available in most of the world including the US, but under strict controls.

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SINthetic Pharmaceutical = ‘Poison of the Witch’

1999 Withdrawn because of risk Trovafloxacin (Trovan) - European Union, US of liver failure[2][3] 2001

Serious gastrointestinal adverse events; ischemic colitis; severe (Lotronex) 2000 US constipation.[2] Reintroduced 2002 on a restricted basis[citation needed]

Risk of fatal cardiac (Propulsid) 2000 US arrhythmias[2]

Phenylpropanolamine(Propage 2000 Canada, US Hemorrhagic stroke.[34][35] st,Dexatrim)

[2] Troglitazone (Rezulin) 2000 US, Germany Hepatotoxicity

Not for reasons of safety or Ardeparin (Normiflo) 2001 US efficacy.[7]

Cerivastatin (Baycol, Lipobay) 2001 US Risk of rhabdomyolysis[2]

Withdrawn in many countries Rapacuronium (Raplon) 2001 US, multiple markets because of risk of fatalbronchospasm[2]

QT prolongation and

Sparfloxacin 2001 US phototoxicity.[2]

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SINthetic Pharmaceutical = ‘Poison of the Witch’

[12] Kava Kava 2002 Germany Hepatotoxicity.

Cardiac arrhythmias and

Levomethadyl acetate 2003 US cardiac arrest.[2]

[8] Bezitramide 2004 Netherlands Fatal overdose.

Co-proxamol (Distalgesic) 2004 UK Overdose dangers.

Drug interactions, prolonged

Dofetilide 2004 Germany QT.[12]

withdrawn by MAH. Risk Rofecoxib (Vioxx) 2004 Worldwide of myocardial infarction and stroke[2]

Risk of heart attack and Valdecoxib (Bextra) 2004 US stroke.[2]

Risk of stroke[1] The ban was later lifted because the death rate among those taking XR 2005 Canada Adderall XR was determined to be no greater than those not taking Adderall.

High risk of accidental Hydromorphone (Palladone, overdose when extended 2005 extended release version) release version (Palladone) administered with . Standard hydromorphone is

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SINthetic Pharmaceutical = ‘Poison of the Witch’

sold in most of the world including the US

Voluntarily withdrawn from US market because of risk 2005 ofProgressive multifocal Natalizumab (Tysabri) – US leukoencephalopathy (PML). 2006 Returned to market July, 2006.

Withdrawn worldwide due to (Melleril) 2005 Germany, UK severe cardiac arrhythmias[54][55]

Liver toxicity; serious liver

Alatrofloxacin 2006 Worldwide injury leading to liver transplant; death.[2]

Increased risk of

Gatifloxacin 2006 US dysglycemia.[2]

Ximelagatran (Exanta) 2006 Germany Hepatotoxicity[12]

Ventricular arrhythmia, QT-

Clobutinol 2007 Germany prolongation.[12]

2007 Lumiracoxib (Prexige) – Worldwide Liver damage 2008

Branded version withdrawn 2007 US, Canada, others by originator in several

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SINthetic Pharmaceutical = ‘Poison of the Witch’

countries in 2007 for hepatotoxicity. Generic versions available.[28]

Risk for heart valve (Permax) 2007 US damage.[2]

Risk for heart attack, stroke, and unstable angina.[2] Was (Zelnorm) 2007 US available through a restricted access program until April 2008.

Aprotinin (Trasylol) 2008 US Increased risk of death.[2]

Risk of severe depression (Acomplia) 2008 Worldwide and suicide[12]

Withdrawn because of increased risk of progressive Efalizumab (Raptiva) 2009 Germany multifocal leukoencephalopathy[12]

Propoxyphene (Darvocet/Darv Increased risk of heart 2010 Worldwide on) attacks and stroke.[14]

Gemtuzumab No improvement in clinical 2010 US ozogamicin(Mylotarg) benefit; risk for death.[2]

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SINthetic Pharmaceutical = ‘Poison of the Witch’

No improvement in clinical

Ozogamicin 2010 US benefit; risk for death; veno- occlusive disease.[2]

Risk of heart attacks and Rosiglitazone (Avandia) 2010 Europe death. This drug continues to be available in the US

Australia,[39] Canada,[40] C hina,[41] the European Union (EU),[42] Hong Kong,[43] India,[44] Mexico, Increased risk of heart attack (Reductil/Meridia) 2010 New Zealand,[45] the and stroke.[2] Philippines,[46] Thailand,[47] the United Kingdom,[48] and the United States[49]

[12] Sitaxentan 2010 Germany Hepatotoxicity.

Lack of efficacy as shown by Drotrecogin alfa (Xigris) 2011 Worldwide PROWESS-SHOCK study[17][18][19]

Serious cutaneous

Tetrazepam 2013 European Union reactions.[51]

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SINthetic Pharmaceutical = ‘Poison of the Witch’ Unapproved Prescription Cough, Cold, and Allergy Products  SHARE  TWEET  LINKEDIN  PIN IT  EMAIL  PRINT The drug products on this list were obtained from the Drug Registration and Listing System (DRLS) in December 2010. For more DRLS Information.

Domestic and foreign establishments that manufacture, repack, or re-label drug products in the United States are required to register and list all of their commercially marketed drug products with the FDA (21 U.S.C. § 360 and 21 CFR 207). Many drug firms do not update their drug listing information with FDA as required by law; consequently, the information in DRLS is both over- and under-inclusive. Therefore, the list below of unapproved prescription cough/cold/allergy drug products may include drugs that are no longer being marketed and/or may not include prescription cough/cold/allergy drug products that are currently being marketed if the drug firm has not listed or updated their information with DRLS. Any unapproved prescription oral cough/cold/allergy drugs that are not on this list are not entitled to any grace period and are subject to immediate enforcement action.

** Incomplete information was submitted to FDA's Drug Registration and Listing system

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

A TAN 12X SUSPENSION PYRILAMINE TANNATE 30 MG 65162 0530

PHENYLEPHRINE TANNATE 5 MG

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

ACCUHIST DM GUAIFENESIN 50 MG 66346 0111

DEXTROMETHORPHAN 5 MG

PSEUDOEPHEDRINE 30 MG

BROMPHENIRAMINE 2 MG

ACCUHIST DROPS CHERRY CHLORPHENIRAMINE MALEATE 0.8 MG 23589 0004 FLAVOR

PSEUDOEPHEDRINE 9 MG HYDROCHLORIDE

AEROHIST CAPLETS EXTENDED CHLORPHENIRAMINE MALEATE 8 MG 038739 *082 RELEASE

METHSCOPOLAMINE NITRATE 2.5 MG

AEROHIST EXTENDED RELEASE CHLORPHENIRAMINE 8 MG 66440 0082 TABLETS

METHSCOPOLAMINE NITRATE 2.5 MG

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

AEROHIST PLUS EXTENDED CHLORPHENIRAMINE MALEATE 8 MG 066440 2376 RELEASE CAPLETS

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

AH CHEW SUSPENSION CHLORPHENIRAMINE TANNATE 35 MG 59196 0015

PHENYLEPHRINE TANNATE 25 MG

AH CHEW ULTRA CHEWABLE CHLORPHENIRAMINE TANNATE 10 MG 59196 0115 TABLET

PHENYLEPHRINE TANNATE 2 MG

AH-CHEW ULTRA PHENYLEPHRINE 2 MG/5ML 59196 0118

CHLORPHENIRAMINE 10 MG/5ML

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

METHSCOPOLAMINE 1.5 MG/5ML

ALAHIST LQ LIQUID 25 MG 50991 0607 HYDROCHLORIDE

PHENYLEPHRINE 7.5 MG HYDROCHLORIDE

ALBATUSSIN NN ALCOHOL FREE DEXTROMETHORPHAN 10 MG 49326 0289 HYDROBROMIDE

PYRILAMINE MALEATE 8.85 MG

POTASSIUM 75 MG GUAIACOLSULFONATE

PHENYLEPHRINE 5 MG HYDROCHLORIDE

ALDEX D TANNATE FOR ORAL PHENYLEPHRINE 5 MG 65224 0550 SUSPENSION HYDROCHLORIDE

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

ALDEX DM FOR ORAL PHENYLEPHRINE 5 MG 65224 0555 SUSPENSION HYDROCHLORIDE

PYRILAMINE MALEATE 16 MG

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

ALDEX DM FOR ORAL DEXTROMETHORPHAN 15 MG 65224 0555 SUSPENSION HYDROBROMIDE

ALDEX TABLETS GUAIFENESIN 650 MG 65224 0650

PHENYLEPHRINE 25 MG

ALLERGY DN II CHLORPHENIRAMINE 4 MG 51991 0534

METHSCOPOLAMINE NITRATE 2.5 MG

METHSCOPOLAMINE NITRATE 2.5 MG 10122 0650

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

ALLERX 10 DAY DOSEPACK PSEUDOEPHEDRINE 120 MG TABLETS HYDROCHLORIDE

ALLERX D TABLETS METHSCOPOLAMINE NITRATE 2.5 MG 10122 *702

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

ALLERX DOSE PACK DF 30 CHLORPHENIRAMINE MALEATE 4 MG 10122 0704 TABLETS

METHSCOPOLAMINE NITRATE 2.5 MG

ALLERX DOSE PACK PE 30 METHSCOPOLAMINE NITRATE 2.5 MG 10122 *705 TABLETS

PHENYLEPHRINE 40 MG HYDROCHLORIDE

ALLERX DOSEPACK TABLETS CHLORPHENIRAMINE MALEATE 8 MG 54868 5198

METHSCOPOLAMINE NITRATE 2.5 MG

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

ALLFEN DM GUAIFENESIN 400 MG 58605 0401

DEXTROMETHORPHAN 20 MG

ALLRES G TANNATE GUAIFENESIN 200 MG 028595 0602 SUSPENSION

CARBETAPENTANE CITRATE 7.5 MG

AMBIFED GUAIFENESIN 400 MG 58605 0414

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

AMBIFED DM GUAIFENESIN 400 MG 58605 0415

DEXTROMETHORPHAN 20 MG

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 30 MG

AQUATAB C DEXTROMETHORPHAN 60 MG 63824 0063

GUAIFENESIN 1200 MG

PHENYLEPHRINE 75 MG

AQUATAB C 12 HOUR TIME DEXTROMETHORPHAN 25 MG 16881 *120 RELEASE TABLETS HYDROBROMIDE

GUAIFENESIN 600 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

AQUATAB DM TABLETS DEXTROMETHORPHAN 60 MG 063824 *002 EXTENDED RELEASE HYDROBROMIDE

GUAIFENESIN 1200 MG

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

B VEX D SUSPENSION BROMPHENIRAMINE TANNATE 12 MG 68308 0926

PHENYLEPHRINE TANNATE 20 MG

B VEX SUSPENSION BROMPHENIRAMINE TANNATE 12 MG 68308 0922

BEN TANN SUSPENSION DIPHENHYDRAMINE TANNATE 25 MG 68308 0122

BETATAN SUSPENSION CARBETAPENTANE TANNATE 30 MG 66992 0125

BROMPHENIRAMINE TANNATE 4 MG

PHENYLEPHRINE TANNATE 7.5 MG

BIODEC DM DROPS DEXTROMETHORPHAN 4 MG 59741 0134 HYDROBROMIDE

PSEUDOEPHEDRINE 25 MG HYDROCHLORIDE

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

BIOTUSS GUAIFENESIN 300 MG 58552 0113

DEXTROMETHORPHAN 15 MG

PHENYLEPHRINE 10 MG

BP 8 GUAIFENESIN 175 MG 42192 0507

DEXTROMETHORPHAN 15 MG

PSEUDOEPHEDRINE 30 MG

BPM PE DM SYRUP BROMPHENIRAMINE MALEATE 2 MG 64376 736

PHENYLEPHRINE 5 MG HYDROCHLORIDE

DEXTROMETHORPHAN 10 MG HYDROBROMIDE

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

BPM PSEUDOEPHERINE BROMPHENIRAMINE MALEATE 6 MG 064376 *544 EXTENDED RELEASE TABLET

PSEUDOEPHEDRINE 45 MG HYDROCHLORIDE

BPM TABLETS BROMPHENIRAMINE MALEATE 6 MG 064376 *543

BROFED ELIXIR PSEUDOEPHEDRINE 30 MG 00682 7777 HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 4 MG

BROMAAPHEDRINE D PHENYLEPHRINE TANNATE 20 MG 68032 0157 SUSPENSION

BROMPHENIRAMINE TANNATE 12 MG

BROMFED CAPSULES BROMPHENIRAMINE MALEATE 12 MG 054868 1211

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

BROMFED CAPSULES PHENYLEPHRINE 15 MG 67000 0200

BROMPHENIRAMINE 12 MG

BROMHIST DM PEDIATRIC BROMPHENIRAMINE MALEATE 2 MG 60258 0446 SYRUP

GUAIFENESIN 50 MG

DEXTROMETHORPHAN 5 MG HYDROBROMIDE

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

BROMPHENIRAMINE MALEATE BROMPHENIRAMINE MALEATE 1 MG 68032 0324 DROPS

BROMPHENIRAMINE MALEATE PSEUDOEPHEDRINE 7.5 MG 68032 0325 PSEUDOEPHEDRINE HCL DROPS HYDROCHLORIDE

DEXBROMPHENIRAMINE 1 MG MALEATE

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SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

BROMPHENIRAMINE BROMPHENIRAMINE 6 MG 62559 6331 PHENYLEPHRINE TANNATE SUSPENSION

PHENYLEPHRINE 10 MG HYDROCHLORIDE

BROMPHENIRAMINE TANNATE BROMPHENIRAMINE TANNATE 12 MG 68013 0007 CHEWABLE TABLETS

BROMPHENIRAMINE TANNATE BROMPHENIRAMINE TANNATE 12 MG 62559 6291 SUSPENSION

BROMPHERIRAMINE TANNATE BROMPHENIRAMINE 12 MG 062559 6293 TABLETS

BROMSPIRO LIQUID DOXYLAMINE SUCCINATE 2.5 MG 23359 0010

BROMTUSS DM LIQUID BROMPHENIRAMINE MALEATE 2 MG 51991 0443 FORMULA

DEXTROMETHORPHAN 15 MG

PHENYLEPHRINE 7.5 MG HYDROCHLORIDE

49

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

BROMUPHED CAPSULES TIME BROMPHENIRAMINE MALEATE 12 MG 00603 2505 RELEASE

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

BROMUPHED PD CAPSULES BROMPHENIRAMINE MALEATE 6 MG 00603 2506 TIME RELEASE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

BRONKIDS LIQUID PHENYLEPHRINE 1.5 MG 49963 0118 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 0.6 MG

DEXTROMETHORPHAN 2.75 MG HYDROBROMIDE

BRONTUSS SF GUAIFENESIN 350 MG 49963 0813

DEXTROMETHORPHAN 15 MG

50

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 10 MG

BROVEX ADT SUSPENSION BROMPHENIRAMINE TANNATE 12 MG 58605 0274

PHENYLEPHRINE TANNATE 10 MG

BROVEX CT BROMPHENIRAMINE TANNATE 12 MG 66813 0273

BROVEX D SUSPENSION BROMPHENIRAMINE TANNATE 12 MG 66813 0274

PHENYLEPHRINE TANNATE 20 MG

BROVEX PD SUSPENSION BROMPHENIRAMINE TANNATE 6 MG 58605 0277

PSEUDOEPHEDRINE TANNATE 30 MG

BROVEX PEB DM LIQUID PHENYLEPHRINE 10 MG 58605 0153 HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 4 MG

51

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

BROVEX PEB LIQUID PHENYLEPHRINE 10 MG 58605 0152 HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 4 MG

BROVEX PSB DM LIQUID BROMPHENIRAMINE MALEATE 4 MG 58605 0151

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

PSEUDOEPHEDRINE 20 MG HYDROCHLORIDE

BROVEX PSB LIQUID BROMPHENIRAMINE MALEATE 4 MG 58605 0150

PSEUDOEPHEDRINE 20 MG HYDROCHLORIDE

BROVEX SR CAPSULES BROMPHENIRAMINE MALEATE 9 MG 66813 *271

52

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 90 MG HYDROCHLORIDE

C PHEN DM DROPS CHLORPHENIRAMINE MALEATE 1 MG 21695 0625

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

PHENYLEPHRINE 3.5 MG HYDROCHLORIDE

C PHEN DM DROPS CHLORPHENIRAMINE MALEATE 1 MG 64376 0726

PHENYLEPHRINE 3.5 MG HYDROCHLORIDE

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

C PHEN DM SYRUP DEXTROMETHORPHAN 15 MG 64376 0727 HYDROBROMIDE

53

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 12.5 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

C PHEN DROPS CHLORPHENIRAMINE MALEATE 1 MG 64376 0728

PHENYLEPHRINE 3.5 MG HYDROCHLORIDE

C PHEN SYRUP PHENYLEPHRINE 12.5 MG 64376 0729 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

C TAN D PLUS SUSPENSION BROMPHENIRAMINE TANNATE 5 MG 23359 0007

PHENYLEPHRINE TANNATE 5 MG

C TAN D SUSPENSION BROMPHENIRAMINE TANNATE 4 MG 23359 0006

54

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE TANNATE 5 MG

C TANNA 12D SUSPENSION PHENYLEPHRINE TANNATE 5 MG 66993 0553

PYRILAMINE TANNATE 30 MG

CARBETAPENTANE TANNATE 30 MG

CARBA XP SYRUP CARBETAPENTANE CITRATE 20 MG 58809 0303

GUAIFENESIN 100 MG

CARBATAB 12 TABLETS CARBETAPENTANE CITRATE 60 MG 58809 *615

GUAIFENESIN 600 MG

PHENYLEPHRINE 15 MG HYDROCHLORIDE

CARBETAPENTANE CITRATE 20 MG 58809 0707

55

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 10 MG HYDROCHLORIDE CARBATUSS CL LIQUID RASPBERRY MINT FLAVOR POTASSIUM 100 MG GUAIACOLSULFONATE

CARBATUSS SYRUP CARBETAPENTANE CITRATE 20 MG 58809 0536

GUAIFENESIN 100 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

CARBODEX DM DROPS PSEUDOEPHEDRINE 15 MG 55654 0028 HYDROCHLORIDE

DEXTROMETHORPHAN 4 MG HYDROBROMIDE

CARBODEX DM DROPS DEXTROMETHORPHAN 4 MG 55654 0015 PEDIATRIC HYDROBROMIDE

56

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 25 MG HYDROCHLORIDE

CARBODEX DM SYRUP DEXTROMETHORPHAN 15 MG 55654 0016 HYDROBROMIDE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

CARBOFED DM DROPS PSEUDOEPHEDRINE 25 MG 50383 0750 HYDROCHLORIDE

DEXTROMETHORPHAN 4 MG HYDROBROMIDE

CARBOFED DM ORAL DROPS PSEUDOEPHEDRINE 15 MG 50383 0576 HYDROCHLORIDE

DEXTROMETHORPHAN 4 MG HYDROBROMIDE

CARBOFED DM SYRUP DEXTROMETHORPHAN 15 MG 50383 0751 HYDROBROMIDE

57

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

CARDEC DM DROPS PSEUDOEPHEDRINE 25 MG 00603 1060 HYDROCHLORIDE

DEXTROMETHORPHAN 4 MG HYDROBROMIDE

CARDEC DM DROPS DEXTROMETHORPHAN 4 MG 00603 1064 HYDROBROMIDE

PSEUDOEPHEDRINE 15 MG HYDROCHLORIDE

CARDEC DM ORAL DROPS DEXTROMETHORPHAN 3 MG 00603 1068 HYDROBROMIDE

PHENYLEPHRINE 3.5 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 1 MG

58

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

CARDEC DM SYRUP DEXTROMETHORPHAN 15 MG 00603 1061 HYDROBROMIDE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

CARDEC DM SYRUP PHENYLEPHRINE 12.5 MG 00603 1069 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

CARDEC ORAL DROPS PHENYLEPHRINE 3.5 MG 00603 1066 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 1 MG

CARDEC SYRUP BROMPHENIRAMINE MALEATE 4 MG 00603 1063

59

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 45 MG HYDROCHLORIDE

CARDEC SYRUP PHENYLEPHRINE 12.5 MG 00603 1067 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

CENTERGY DM PEDIATRIC CHLORPHENIRAMINE MALEATE 1 MG 23359 0015 DROPS

PHENYLEPHRINE 2 MG HYDROCHLORIDE

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

CENTERGY PEDIATRIC DROPS PHENYLEPHRINE 2 MG 23359 0014 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 1 MG

CERON DM SYRUP CHLORPHENIRAMINE MALEATE 4 MG 60258 0415

60

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 12.5 MG HYDROCHLORIDE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

CERON SYRUP PHENYLEPHRINE 12.5 MG 60258 0414 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

CERTUSS D SUSTAINED RELEASE DEXTROMETHORPHAN 60 MG 64543 *175 TABLETS HYDROBROMIDE

GUAIFENESIN 600 MG

PHENYLEPHRINE 40 MG HYDROCHLORIDE

CERTUSS MULTILAYER CARBETAPENTANE CITRATE 60 MG 64543 *180 EXTENDED RELEASE TABLET

GUAIFENESIN 1200 MG

61

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

CHLOR MES D LIQUID METHSCOPOLAMINE NITRATE 0.625 MG 60258 0221

PHENYLEPHRINE 10 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

CHLOR PSEUDO CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 00440 8255 EXTENDED RELEASE

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

CHLORDEX GP SYRUP CHLORPHENIRAMINE MALEATE 2 MG 60258 0246

GUAIFENESIN 100 MG

DEXTROMETHORPHAN 7.5 MG HYDROBROMIDE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

62

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

CHLORFED A SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 55289 *284

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE CHLORPHENIRAMINE MALEATE 8 MG 00185 1304 AND PSEUDOEPHEDRINE HYDROCHLORIDE CAPSULES EXTENDED RELEASE PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE CHLORPHENIRAMINE MALEATE 8 MG 00603 2784 CAPSULES EXTENDED RELEASE

CHLORPHENIRAMINE MALEATE CHLORPHENIRAMINE MALEATE 12 MG 00603 2785 CAPSULES EXTENDED RELEASE

CHLORPHENIRAMINE PHENYLEPHRINE 12.5 MG 54569 5803 PHENYLEPHRINE DM SYRUP HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

63

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

COLDAMINE TABLETS CHLORPHENIRAMINE MALEATE 8 MG 10149 *229

METHSCOPOLAMINE NITRATE 2.5 MG

PSEUDOEPHEDRINE 90 MG HYDROCHLORIDE

COLDMIST DM TABLETS DEXTROMETHORPHAN 32 MG 51991 *146 EXTENDED RELEASE HYDROBROMIDE

GUAIFENESIN 595 MG

PSEUDOEPHEDRINE 48 MG HYDROCHLORIDE

COLDMIST LA EXTENDED GUAIFENESIN 795 MG 51991 *367 RELEASE TABLETS

PSEUDOEPHEDRINE 85 MG HYDROCHLORIDE

64

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

COLFED A CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 51991 *145

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

CORFEN DM LIQUID PHENYLEPHRINE 10 MG 60258 0238 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

CORYZA D TABLETS DEXCHLORPHENIRAMINE 3.5 MG 68047 *271 MALEATE

PSEUDOEPHEDRINE 45 MG

METHSCOPOLAMINE NITRATE 1 MG

CORYZA DM SYRUP PHENYLEPHRINE 5 MG 68047 0270 HYDROCHLORIDE

65

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXCHLORPHENIRAMINE 1.25 MG MALEATE

DEXTROMETHORPHAN 5 MG HYDROBROMIDE

PYRILAMINE MALEATE 5 MG

CORZALL LIQUID PSEUDOEPHEDRINE 30 MG 63717 0552 HYDROCHLORIDE

CARBETAPENTANE CITRATE 20 MG

CP DEC DM ORAL DROPS CHLORPHENIRAMINE MALEATE 1 MG 50383 0873

PHENYLEPHRINE 3.5 MG HYDROCHLORIDE

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

CP DEC DM SYRUP CHLORPHENIRAMINE MALEATE 4 MG 50383 0872

66

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 12.5 MG HYDROCHLORIDE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

CP DEC ORAL DROPS CHLORPHENIRAMINE MALEATE 1 MG 50383 0871

PHENYLEPHRINE 3.5 MG HYDROCHLORIDE

C-PHEN DM DEXTROMETHORPHAN 3 MG 23490 7848 HYDROBROMIDE

PHENYLEPHRINE 3 MG

CHORPHENIRAMINE MALEATE 1 MG

CPM PSE SYRUP PSEUDOEPHEDRINE 30 MG 64376 0714 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

67

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

CYPROHEPTADINE HCL HCL 4 MG 00440 7360

D TAB SUSTAINED RELEASE GUAIFENESIN 1200 MG 24518 *001 TABLETS

PHENYLEPHRINE 40 MG HYDROCHLORIDE

DA CHEWABLE TABLETS METHSCOPOLAMINE NITRATE 1.25 MG 64455 0013

CHLORPHENIRAMINE MALEATE 2 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

DALLERGY CAPLETS CHLORPHENIRAMINE 12 MG 00277 0182

PHENYLEPHRINE 20 MG

METHSCOPOLAMINE NITRATE 2.5 MG

68

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DALLERGY DROPS PHENYLEPHRINE 2 MG 16477 0120 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 1 MG

DALLERGY JR CAPSULES PHENYLEPHRINE 20 MG 00277 0183

CHLORPHENIRAMINE 4 MG

DALLERGY PE SYRUP CHLORPHENIRAMINE MALEATE 2 MG 16477 0821

METHSCOPOLAMINE NITRATE 0.75 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

DALLERGY PSE ER TABLETS PSEUDOEPHEDRINE 60 MG 16477 0146

CLORPHENIRAMINE 4 MG

69

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

METHSCOPOLAMINE NITRATE 1.25 MG

DALLERGY SYRUP METHSCOPOLAMINE NITRATE 0.75 MG 16477 0819

PHENYLEPHRINE 8 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

DALLERGY TABLETS METHSCOPOLAMINE NITRATE 1.25 MG 00277 0160

PHENYLEPHRINE 10 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

DE CHLOR DM LIQUID PHENYLEPHRINE 10 MG 60258 0239 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

70

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

DE CHLOR DR LIQUID CHLORPHENIRAMINE MALEATE 2 MG 60258 0240

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

PHENYLEPHRINE 6 MG HYDROCHLORIDE

DE CONGESTINE SUSTAINED CHLORPHENIRAMINE 8 MG 00603 3143 RELEASE CAPSULES

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

DECON E LIQUID GUAIFENESIN 100 MG 51724 0014

PHENYLEPHRINE 5 MG HYDROCHLORIDE

DECON G DROPS GUAIFENESIN 40 MG 51724 0214

71

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 2 MG HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 1 MG

DECONAMINE SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 54868 1014

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

DECONAMINE SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 00482 0181 SUSTAINED RELEASE

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

DECONAMINE SYRUP PSEUDOEPHEDRINE 30 MG 00482 0185 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

DECONAMINE TABLETS PSEUDOEPHEDRINE 60 MG 00482 0184 HYDROCHLORIDE

72

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

CHLORPHENIRAMINE MALEATE 4 MG

DECONEX TABLETS GUAIFENESIN 900 MG 50991 *306

PHENYLEPHRINE 30 MG HYDROCHLORIDE

DECONGEST II TABLETS GUAIFENESIN 600 MG 00603 3116

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

DECONOMED SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 61646 *300

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

DEFEN LA TABLETS GUAIFENESIN 600 MG 59630 *110

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

73

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEX PC SYRUP PHENYLEPHRINE 6 MG 64376 0711 HYDROCHLORIDE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

CHLORPHENIRAMINE MALEATE 2 MG

DEXCHLORPHENIRAMINE DEXCHLORPHENIRAMINE 4 MG 00591 4008 MALEATE TABLETS MALEATE

DEXCHLORPHENIRAMINE DEXCHLORPHENIRAMINE 4 MG 00603 3198 MALEATE TABLETS MALEATE

DEXCHLORPHENIRAMINE DEXCHLORPHENIRAMINE 6 MG 00603 3199 MALEATE TABLETS MALEATE

DEXODRYL CHEWABLE TABLET CHLORPHENIRAMINE TANNATE 2 MG 59196 0117

DEXODRYL SUSPENSION CHLORPHENIRAMINE TANNATE 2 MG 59196 0116

DEXPHEN M ORAL SOLUTION METHSCOPOLAMINE NITRATE 1.25 MG 64376 0737

74

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXCHLORPHENIRAMINE 1 MG MALEATE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

DEXTRO PHENYL PYRIL LIQUID PHENYLEPHRINE 15.5 MG 68032 0327

PYRILAMINE 15.5 MG

DEXTROMETHORPHAN HBR DEXTROMETHORPHAN 15 MG 68032 0168 CHLORPHENIRAMINE MALEATE HYDROBROMIDE PHENYLEPHRINE HCL LIQUID

PHENYLEPHRINE 10 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

DEXTROMETHORPHAN DEXTROMETHORPHAN 30 MG 68032 0307 TANNATE PHENYLEPHRINE TANNATE

PHENYLEPHRINE 20 MG

75

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXCHLORPHENIRAMINE TANNATE DEXCHLORPHENIRAMINE 2 MG

DHISTINE SYRUP PHENYLEPHRINE 10 MG 60258 0220 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

METHSCOPOLAMINE NITRATE 1.25 MG

DIPHENMAX TABLETS DIPHENHYDRAMINE TANNATE 25 MG 68032 0189 CHEWABLE

DONATUSSIN DM DROPS PHENYLEPHRINE 1.5 MG 16477 0811 HYDROCHLORIDE

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

CHLORPHENIRAMINE MALEATE 1 MG

DONATUSSIN DM SUSPENSION DEXTROMETHORPHAN 30 MG 16477 0130 TANNATE

76

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE TANNATE 20 MG

DEXCHLORPHENIRAMINE 2 MG TANNATE

DONATUSSIN DROPS GUAIFENESIN 20 MG 16477 0106

PHENYLEPHRINE 1.5 MG HYDROCHLORIDE

DONTATUSSIN DM SYRUP GUAIFENESIN 150 MG 16477 0132

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

DOXYTEX SYRUP DOXYLAMINE SUCCINATE 2.5 MG 23359 0011

DRIHIST SR TABLETS CHLORPHENIRAMINE MALEATE 8 MG 066993 *110

77

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

DRITUSS DM ELIXIR GUAIFENESIN 200 MG 00603 1181

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

DRITUSS GF TABLETS GUAIFENESIN 1200 MG 00603 3504

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

DRYSEC TABLETS CHLORPHENIRAMINE MALEATE 8 MG 12539 *727

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

78

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DURA VENT DA TABLETS CHLORPHENIRAMINE MALEATE 8 MG 64455 *008

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

DURADRYL CHEWABLE TABLETS METHSCOPOLAMINE NITRATE 1.25 MG 51991 0591

CHLORPHENIRAMINE MALEATE 2 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

DURAVENT DA TABLETS CHLORPHENIRAMINE MALEATE 8 MG 33753 *101 EXTENDED RELEASE

PHENYLEPHRINE 20 MG HYDROCHLORIDE

METHSCOPOLAMINE NITRATE 2.5 MG

79

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DURAVENT DPB SYRUP PHENYLEPHRINE 5 MG 33753 0105 HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 2 MG

DEXTROMETHORPHAN 10 MG HYDROBROMIDE

DYNAHIST ER CAPSULES CHLORPHENIRAMINE MALEATE 4 MG 51991 *217 PEDIATRIC

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

DYNATUSS-EX GUAIFENESIN 200 MG 51991 0211

DEXTROMETHORPHAN 30 MG

PHENYLEPHRIN 10 MG

DYNEX 12 SUSPENSION CARBETAPENTANE TANNATE 22.5 MG 66813 0038

80

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE TANNATE 9 MG

DYNEX TABLETS GUAIFENESIN 1200 MG 66813 *033

PSEUDOEPHEDRINE 90 MG HYDROCHLORIDE

ED A HIST DM LIQUID BANANA CHLORPHENIRAMINE MALEATE 4 MG 00485 0071 FLAVOR

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

ED A HIST LIQUID CHLORPHENIRAMINE MALEATE 4 MG 00485 0055

PHENYLEPHRINE 10 MG HYDROCHLORIDE

ED A-HIST TABLETS CHLORPHENIRAMINE MALEATE 8 MG 00485 0054

81

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 20 MG HYDROCHLORIDE

ED CHLOR TAN CAPLETS CHLORPHENIRAMINE TANNATE 8 MG 00485 0072

ED CHLORPED FOR SUSPENSION CHLORPHENIRAMINE TANNATE 2 MG 00485 0074

ENDACON DM EXTENDED DEXTROMETHORPHAN 30 MG 28595 *100 RELEASE TABLET HYDROBROMIDE

GUAIFENESIN 600 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

ENDAL HD SYRUP CHERRY PHENYLEPHRINE 7.5 MG 23589 *008 FLAVOR HYDROCHLORIDE

DIPHENHYDRAMINE 12.5 MG HYDROCHLORIDE

GUAIFENESIN 800 MG 66813 *535

82

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

ENTEX LA EXTENDED RELEASE PHENYLEPHRINE 30 MG TABLET HYDROCHLORIDE

ENTEX PSE EXTENDED RELEASE GUAIFENESIN 525 MG 66813 *525 TABLET

PSEUDOEPHEDRINE 50 MG HYDROCHLORIDE

ENTEX SUSPENSION PSEUDOEPHEDRINE TANNATE 22.5 MG 66813 0555

EXALL D LIQUID GUAIFENESIN 100 MG 63717 0555

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

CARBETAPENTANE CITRATE 10 MG

EXALL PLUS LIQUID GUAIFENESIN 100 MG 63717 0554

CARBETAPENTANE CITRATE 10 MG

83

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

EXECOF TABLETS DEXTROMETHORPHAN 60 MG 68047 *170 HYDROBROMIDE

GUAIFENESIN 1000 MG

PHENYLEPHRINE 40 MG HYDROCHLORIDE

EXEFEN DM SUSTAINED DEXTROMETHORPHAN 55 MG 68047 *151 RELEASE TABLETS HYDROBROMIDE

GUAIFENESIN 1000 MG

EXEFEN EXTENDED RELEASE DEXTROMETHORPHAN 40 MG 68047 *153 TABLET HYDROBROMIDE

GUAIFENESIN 780 MG

PSEUDOEPHEDRINE 80 MG HYDROCHLORIDE

84

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

EXEFEN IR TABLETS PSEUDOEPHEDRINE 60 MG 68047 0154 HYDROCHLORIDE

GUAIFENESIN 400 MG

EXEFEN PD EXTENDED RELEASE GUAIFENESIN 600 MG 68047 *150 TABLETS

PHENYLEPHRINE 10 MG HYDROCHLORIDE

EXETUSS DM EXTENDED DEXTROMETHORPHAN 25 MG 68047 *183 RELEASE TABLET HYDROBROMIDE

GUAIFENESIN 600 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

EXPECTUSS LIQUID CARBETAPENTANE CITRATE 20 MG 23359 0003

GUAIFENESIN 75 MG

85

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

EXTENDRYL CHEWABLE METHSCOPOLAMINE NITRATE 1.25 MG 14629 0103 TABLETS

PHENYLEPHRINE 10 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

EXTENDRYL GCP ORAL GUAIFENESIN 100 MG 14629 0105 SOLUTION

PHENYLEPHRINE 5 MG HYDROCHLORIDE

CARBETAPENTANE CITRATE 15 MG

EXTENDRYL JR CAPSULES CHLORPHENIRAMINE MALEATE 4 MG 14629 *102

METHSCOPOLAMINE NITRATE 1.25 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

86

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

EXTENDRYL SYRUP DEXCHLORPHENIRAMINE 1 MG 14629 0114 MALEATE

METHSCOPOLAMINE NITRATE 1.25 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

EXTENDRYL TABLETS CHLORPHENIRAMINE MALEATE 8 MG 14629 *101 SUSTAINED RELEASE

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

FENESIN DM TABLETS DEXTROMETHORPHAN 30 MG 64455 *014 HYDROBROMIDE

GUAIFENESIN 600 MG

GANI TUSS DM NR LIQUID DEXTROMETHORPHAN 10 MG 60258 0262 HYDROBROMIDE

87

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

GUAIFENESIN 100 MG

GANIDIN NR LIQUID GUAIFENESIN 100 MG 60258 0256

G-BID DM TR TABLETS DEXTROMETHORPHAN 60 MG 064376 *542 HYDROBROMIDE

GUAIFENESIN 1200 MG

GENETUSS 2 SYRUP GUAIFENESIN 300 MG 65615 0426

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

GENTEX 30 LIQUID CARBETAPENTANE CITRATE 30 MG 15014 0888

GUAIFENESIN 200 MG

88

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 8 MG HYDROCHLORIDE

GENTEX LA TABLETS SUSTAINED GUAIFENESIN 650 MG 15014 *002 RELEASE

PHENYLEPHRINE 23.75 MG HYDROCHLORIDE

GENTEX LQ SYRUP PHENYLEPHRINE 10 MG 15014 0001 HYDROCHLORIDE

CARBETAPENTANE CITRATE 20 MG

GUAIFENESIN 100 MG

GFN 580 PSEH 60 00 EXTENDED GUAIFENESIN 580 MG 58605 0614 RELEASE TABLETS

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

GFN AND DM TABLETS GUAIFENESIN 800 MG 60258 0292

89

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 30 MG

GILTUSS GUAIFENESIN 300 MG 58552 0108

DEXTROMETHORPHAN 15 MG

PHENYLEPHRINE 10 MG

GILTUSS PEDIATRIC GUAIFENESIN 50 58552 0107 MG/1ML

DEXTROMETHORPHAN 5 MG/ML

PHENYLEPHRINE 2.5 MG/ML

GILTUSS TR GUAIFENESIN 288 MG 58552 0312

DEXTROMETHORPHAN 14 MG

90

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 7 MG

G-PHED TIME RELEASE GUAIFENESIN 250 MG 59743 0002 CAPSULES

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

GUAIDEX TR TABLETS CHLORPHENIRAMINE MALEATE 8 MG 66177 *817 EXTENDED RELEASE

DEXTROMETHORPHAN 60 MG HYDROBROMIDE

GUAIFENESIN 1000 MG

METHSCOPOLAMINE NITRATE 1.25 MG

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

GUAIFENESIN 600 MG 00603 3767

91

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

GUAIFEN PSE EXTENDED PSEUDOEPHEDRINE 120 MG RELEASE TABLETS HYDROCHLORIDE

GUAIFEN PSE TABLETS GUAIFENESIN 600 MG 00603 5668

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

GUAIFENESIN AND PHENYLEPHRINE 5 MG 68032 0276 PHENYLEPHRINE HCL SYRUP HYDROCHLORIDE

GUAIFENESIN 200 MG

GUAIFENESIN DM NR LIQUID DEXTROMETHORPHAN 10 MG 54838 0124 HYDROBROMIDE

GUAIFENESIN 100 MG

GUAIFENESIN DM NR LIQUID GUAIFENESIN 100 MG 62305 0400

DEXTROMETHORPHAN 10 MG HYDROBROMIDE

92

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

GUAIFENESIN DM TABLETS DEXTROMETHORPHAN 60 MG 66993 *312 HYDROBROMIDE

GUAIFENESIN 1000 MG

GUAIFENESIN DM TABLETS DEXTROMETHORPHAN 30 MG 51285 *420 SUSTAINED RELEASE HYDROBROMIDE

GUAIFENESIN 600 MG

GUAIFENESIN LA CAPLETS GUAIFENESIN 600 MG 00904 7759

GUAIFENESIN LA TABLETS GUAIFENESIN 600 MG 64376 *501

GUAIFENESIN LA TABLETS GUAIFENESIN 600 MG 51655 0948

GUAIFENESIN NR LIQUID GUAIFENESIN 100 MG 54838 0123

GUAIFENESIN NR LIQUID GUAIFENESIN 100 MG 62305 0401

93

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

GUAIFENESIN SUSTAINED GUAIFENESIN 1200 MG 00603 3773 RELEASE TABLETS

GUAIFENESIN SYRUP ALCOHOL GUAIFENESIN 100 MG 60432 0079 FREE AND SUGAR FREE

GUAIFENESIN TABLETS GUAIFENESIN 200 MG 00904 5154

GUAIFENESIN TABLETS GUAIFENESIN 1000 MG 66993 *320

GUAIFENESIN TABLETS GUAIFENESIN 600 MG 51285 *417 SUSTAINED RELEASE

GUAIFENESIN TR TABLETS GUAIFENESIN 600 MG 61646 *125

GUAIFENSIN LA TABLETS GUAIFENESIN 600 MG 57664 *152

GUAIPHEN-D TR TABLETS GUAIFENESIN 600 MG 64376 *540

PHENYLEPHRINE 40 MG HYDROCHLORIDE

94

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

GUAPHEN II DM TABLETS DEXTROMETHORPHAN 20 MG 68032 *134 EXTENDED RELEASE HYDROBROMIDE

GUAIFENESIN 800 MG

GUIADEX DM LIQUID DEXTROMETHORPHAN 15 MG 51991 0087 HYDROBROMIDE

POTASSIUM 300 MG GUAIACOLSULFONATE

GUIADEX PD EXTENDED GUAIFENESIN 600 MG 51991 *090 RELEASE TABLETS

PHENYLEPHRINE 10 MG HYDROCHLORIDE

GUIADRINE DX LIQUID GUAIFENESIN 225 MG 51991 0633

DEXTROMETHORPHAN 25 MG HYDROBROMIDE

GUIADRINE GP TABLETS GUAIFENESIN 1200 MG 51991 *058

95

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

GUIATEX PE SYRUP GUAIFENESIN 200 MG 51991 0597

PHENYLEPHRINE 5 MG HYDROCHLORIDE

HEXAFED TABLETS DEXCHLORPHENIRAMINE 4 MG 68220 *027 MALEATE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

HISTACOL DM PEDIATRIC GUAIFENESIN 50 MG 51991 0163 SYRUP

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

DEXTROMETHORPHAN 5 MG HYDROBROMIDE

96

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

BROMPHENIRAMINE MALEATE 2 MG

HISTEX LIQUID CHLORPHENIRAMINE MALEATE 2 MG 23589 0002

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

HISTEX LIQUID PSEUDOEPHEDRINE 30 MG 67336 0275 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

HISTEX SR CAPSULES BROMPHENIRAMINE MALEATE 10 MG 67336 *089

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

HT TUSS DM ELIXIR GUAIFENESIN 200 MG 50383 0135

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

97

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

HUMIBID DM TABLETS GUAIFENESIN 600 MG 52959 0129

DEXTROMETHORPHAN 30 MG

HYDRO PRO DM SR TABLETS DEXTROMETHORPHAN 30 MG 51991 *243 HYDROBROMIDE

GUAIFENESIN 600 MG

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

IOBID DM TABLETS DEXTROMETHORPHAN 30 MG 61646 *112 HYDROBROMIDE

GUAIFENESIN 600 MG

IOPHEN DM NR LIQUID GUAIFENESIN 100 MG 00254 9232

DEXTROMETHORPHAN 10 MG HYDROBROMIDE

98

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

IOPHEN DM NR LIQUID GUAIFENESIN 100 MG 00603 1330

DEXTROMETHORPHAN 10 MG HYDROBROMIDE

IOPHEN NR LIQUID GUAIFENESIN 100 MG 00603 1328

J MAX SYRUP PHENYLEPHRINE 5 MG 64661 0011 HYDROCHLORIDE

GUAIFENESIN 200 MG

J MAX TABLETS GUAIFENESIN 1200 MG 64661 *010

PHENYLEPHRINE 35 MG HYDROCHLORIDE

J TAN D PD ORAL DROPS BROMPHENIRAMINE MALEATE 1 MG 64661 0032

PSEUDOEPHEDRINE 7.5 MG HYDROCHLORIDE

99

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

J TAN D SR TABLETS BROMPHENIRAMINE MALEATE 6 MG 64661 *050

PHENYLEPHRINE 30 MG HYDROCHLORIDE

J TAN D SUSPENSION PHENYLEPHRINE TANNATE 5 MG 64661 0022

BROMPHENIRAMINE TANNATE 4 MG

J TAN D TABLETS CHEWABLE PHENYLEPHRINE TANNATE ** ** 64661 0021

BROMPHENIRAMINE TANNATE ** **

J TAN PD ORAL DROPS BROMPHENIRAMINE MALEATE 1 MG 64661 0031

J TAN SUSPENSION BROMPHENIRAMINE TANNATE 4 MG 64661 0020

LARTUS GUAIFENESIN ** ** 58173 0037

DEXTROMETHORPHAN ** **

100

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE ** **

LEV PSE AND GG EXTENDED GUAIFENESIN 400 MG 67537 *035 RELEASE CAPSULES

PSEUDOEPHEDRINE 90 MG HYDROCHLORIDE

LEVALL 12 ORAL SUSPENSION PHENYLEPHRINE TANNATE 25 MG 14629 0304

CARBETAPENTANE TANNATE 30 MG

LEVALL 12 SUSPENSION CARBETAPENTANE TANNATE 30 MG 66813 0180

PHENYLEPHRINE TANNATE 30 MG

LEVALL 12 SUSPENSION PHENYLEPHRINE TANNATE 30 MG 67537 0180

CARBETAPENTANE TANNATE 30 MG

101

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

LEVALL LIQUID PHENYLEPHRINE 15 MG 66813 0179 HYDROCHLORIDE

GUAIFENESIN 100 MG

CARBETAPENTANE CITRATE 20 MG

LIQUIBID PD TABLETS GUAIFENESIN 275 MG 64543 *146

PHENYLEPHRINE 25 MG HYDROCHLORIDE

LIQUICOUGH DM LIQUID PSEUDOEPHEDRINE 32 MG 51991 0646 HYDROCHLORIDE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

GUAIFENESIN 175 MG

LODRANE 12 D TABLETS BROMPHENIRAMINE MALEATE 6 MG 00095 0645

102

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 45 MG HYDROCHLORIDE

LODRANE 12 HOUR TABLETS BROMPHENIRAMINE MALEATE 6 MG 00095 0006 EXTENDED RELEASE

LODRANE 24 HOUR EXTENDED BROMPHENIRAMINE MALEATE 12 MG 00095 1200 RELEASE CAPSULES

LODRANE 24D CAPSULES BROMPHENIRAMINE MALEATE 12 MG 00095 1290 EXTENDED RELEASE

PSEUDOEPHEDRINE 90 MG HYDROCHLORIDE

LODRANE D SUSPENSION PSEUDOEPHEDRINE TANNATE 90 MG 00095 9008

LOHIST 12D TABLETS EXTENDED BROMPHENIRAMINE MALEATE 6 MG 68047 *122 RELEASE

PSEUDOEPHEDRINE 45 MG HYDROCHLORIDE

103

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

LOHIST DM SYRUP DEXTROMETHORPHAN 10 MG 68047 0129 HYDROBROMIDE

BROMPHENIRAMINE MALEATE 2 MG

PHENYLEPHRINE 5 MG HYDROCHLORIDE

LOHIST PD PEDIATRIC DROPS PSEUDOEPHEDRINE 12.5 MG 68047 0011 HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 1 MG

LUSONAL LIQUID PHENYLEPHRINE 7.5 MG 66992 0146 HYDROCHLORIDE

LUSONEX TABLETS GUAIFENESIN 800 MG 66992 *140

PHENYLEPHRINE 20 MG HYDROCHLORIDE

MAXIPHEN GUAIFENESIN 400 MG 58605 0422

104

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 10 MG

MAXIPHEN ADT TABLETS CHLORPHENIRAMINE TANNATE 2 MG 66870 0030

DEXTROMETHORPHAN 30 MG TANNATE

PHENYLEPHRINE TANNATE 20 MG

MAXIPHEN DM GUAIFENESIN 400 MG 58605 0423

DEXTROMETHORPHAN 20 MG

PHENYLEPHRINE 10 MG

MAXI-TUSS DM GUAIFENESIN 200 MG 58605 0522

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

105

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

MEDENT DM TABLETS DEXTROMETHORPHAN 30 MG 45985 *641 HYDROBROMIDE

GUAIFENESIN 800 MG

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

MEDENT LD TABLETS GUAIFENESIN 800 MG 45985 *642

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

MINTEX PSEUDOEPHEDRINE 30 51991 0226 HYDROCHLORIDE MG/5ML

CHLORPHENIRAMINE MALEATE 2 MG/5ML

MINTUSS DR LIQUID DEXCHLORPHENIRAMINE 2 MG 51991 0286 MALEATE

106

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

PHENYLEPHRINE 6 MG HYDROCHLORIDE

MONTEPHEN TABLETS GUAIFENESIN 600 MG 12162 *701

PHENYLEPHRINE 25 MG HYDROCHLORIDE

MUCO FEN DM TABLETS DEXTROMETHORPHAN 60 MG 59310 *119 HYDROBROMIDE

GUAIFENESIN 1000 MG

MYHIST DM LIQUID PYRILAMINE MALEATE 12.5 MG 68047 0230

DEXTROMETHORPHAN 15 MG HYDRIODIDE

107

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 7.5 MG HYDROCHLORIDE

NALDEX TABLETS PHENYLEPHRINE 18.5 MG 51674 0307 HYDROCHLORIDE

DEXCHLORPHENIRAMINE 3.5 MG MALEATE

NALEX JR CAPSULES GUAIFENESIN 300 MG 051674 0003

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

NASATAB LA TABLETS GUAIFENESIN 500 MG 00095 0225

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

NASOHIST DM PEDIATRIC PHENYLEPHRINE 2 MG 63717 0291 DROPS HYDROCHLORIDE

108

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

CHLORPHENIRAMINE MALEATE 1 MG

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

NASOHIST PEDIATRIC DROPS PHENYLEPHRINE 2 MG 63717 0290 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 1 MG

NEO DM DROPS CHLORPHENIRAMINE MALEATE 0.75 MG 16477 0620

DEXTROMETHORPHAN 2.75 MG HYDROBROMIDE

PHENYLEPHRINE 1.75 MG HYDROCHLORIDE

NEUTRAHIST DROPS PSEUDOEPHEDRINE 9 MG 60258 0395 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 0.8 MG

109

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

NO HIST CHEWABLE TABLETS CHLORPHENIRAMINE MALEATE 2 MG 68047 0166

METHSCOPOLAMINE NITRATE 1.25 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

NOHIST CAPLETS CHLORPHENIRAMINE MALEATE 8 MG 68047 *160

PHENYLEPHRINE 20 MG HYDROCHLORIDE

NOHIST DMX SUSTAINED CHLORPHENIRAMINE MALEATE 8 MG 68047 *167 RELEASE TABLETS

DEXTROMETHORPHAN 30 MG HYDROBROMIDE

PHENYLEPHRINE 20 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 8 MG 68047 *161

110

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

NOHIST EXT EXTENDED METHSCOPOLAMINE NITRATE 2.5 MG RELEASE CAPLET

NOHIST PLUS JR TABLETS CHLORPHENIRAMINE MALEATE 4 MG 68047 *165

METHSCOPOLAMINE NITRATE 1.25 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

NOHIST PLUS TABLETS CHLORPHENIRAMINE MALEATE 8 MG 68047 *163

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

NOREL EX TABLETS GUAIFENESIN 800 MG 52747 *440

PHENYLEPHRINE 40 MG HYDROCHLORIDE

111

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

NOREL LA & CARBINOXAMINE MALEATE 8 MG 52747 *435 DECONGESTANT TABLETS

PHENYLEPHRINE 40 MG HYDROCHLORIDE

NORTUSS EX LIQUID DEXTROMETHORPHAN 40 MG 51724 0220 HYDROBROMIDE

GUAIFENESIN 400 MG

OMNIHIST II LA TABLETS CHLORPHENIRAMINE MALEATE 8 MG 59196 *032

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

ORATUSS 12 TABLETS GUAIFENESIN 600 MG 067204 *273

CARBETAPENTANE CITRATE 60 MG

112

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 15 MG HYDROCHLORIDE

ORATUSS LIQUID CARBETAPENTANE CITRATE 20 MG 67204 0210

ORGAN I NR TABLETS GUAIFENESIN 200 MG 00603 4886

ORGANIDIN NR LIQUID GUAIFENESIN 100 MG 00037 4214

ORGANIDIN NR TABLETS GUAIFENESIN 200 MG 00037 4312

P CHLOR GG DROPS NASAL CHLORPHENIRAMINE MALEATE 1 MG 64376 0707 DECONGESTANT

GUAIFENESIN 20 MG

PHENYLEPHRINE 2 MG HYDROCHLORIDE

PCM ALLERGY TABLETS CHLORPHENIRAMINE MALEATE 12 MG 64376 *036

113

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

PCM CHEWABLE TABLETS METHSCOPOLAMINE NITRATE 1.25 MG 64376 0530

PHENYLEPHRINE 10 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

PDM GG SYRUP GUAIFENESIN 200 MG 64376 0710

PHENYLEPHRINE 10 MG HYDROCHLORIDE

DEXTROMETHORPHAN 30 MG HYDROBROMIDE

PE HIST DM SYRUP PHENYLEPHRINE 5 MG 68047 0320 HYDROCHLORIDE

114

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

CHLORPHENIRAMINE MALEATE 2 MG

PEDIAHIST DM SYRUP BROMPHENIRAMINE MALEATE 2 MG 64376 0723

GUAIFENESIN 50 MG

DEXTROMETHORPHAN 5 MG HYDROBROMIDE

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

P--GUAIFEN-DM GUAIFENESIN 100 MG 00677 1800

DEXTROMETHOPHAN 15 MG HYDROBROMIDE

PHENYLEPHRINE 45 MG HYDROCHLORIDE

115

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENA S 12 SUSPENSION PHENYLEPHRINE TANNATE 7.5 MG 58809 0912

PYRILAMINE TANNATE 10 MG

PHENABID CHLORPHENIRAMINE MALEATE 8 MG 58552 *305

PHENYLEPHRINE 20 MG HYDROCHLORIDE

PHENABID DM DEXTROMETHORPHAN 30 MG 58552 0306

PHENYLEPHRINE 20 MG

CHLORPHENIRAMINE 8 MG

PHENCARB GG SYRUP CARBETAPENTANE CITRATE 20 MG 64376 0537

GUAIFENESIN 100 MG

116

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

PHENYDEX LIQUID GUAIFENESIN 200 MG 59936 0005

PYRILAMINE MALEATE 8.35 MG

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

PHENYL T SUSPENSION PHENYLEPHRINE TANNATE 7.5 MG 64376 0437

PHENYLEPHRINE CM TR CHLORPHENIRAMINE MALEATE 8 MG 64376 *546 TABLETS

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 40 MG HYDROCHLORIDE

GUAIFENESIN 900 MG 66993 0326

117

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE PHENYLEPHRINE 25 MG HYDROCHLORIDE AND GUAIFENESIN TABLETS

POLY HIST DM LIQUID PHENYLEPHRINE 7.5 MG 50991 0126 HYDROCHLORIDE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

PYRILAMINE MALEATE 12.5 MG

POLY TUSSIN DM COUGH DEXTROMETHORPHAN 15 MG 50991 0320 SYRUP HYDROBROMIDE

PHENYLEPHRINE 5 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

POLY VENT JR CAPLETS GUAIFENESIN 650 MG 50991 *907

118

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 45 MG HYDROCHLORIDE

POLYTAN D SUSPENSION DEXBROMPHENIRAMINE 4 MG 50991 0817 TANNATE

PHENYLEPHRINE TANNATE 2.5 MG

POLYTAN DM SUSPENSION DEXBROMPHENIRAMINE 4 MG 50991 0710 TANNATE

PHENYLEPHRINE TANNATE 25 MG

DEXTROMETHORPHAN 30 MG TANNATE

POLYTAN SUSPENSION DEXBROMPHENIRAMINE 4 MG 50991 0412 TANNATE

POLYVENT CAPLETS GUAIFENESIN 650 MG 50991 0408

PSEUDOEPHEDRINE 90 MG

119

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PRE HIST D TABLETS CHLORPHENIRAMINE MALEATE 8 MG 00682 0100

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

PROLEX DM LIQUID POTASSIUM 300 MG 51674 0019 GUAIACOLSULFONATE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

PROLEX PD TABLETS GUAIFENESIN 600 MG 51674 0126

PHENYLEPHRINE 10 MG

PROSET D TABLETS GUAIFENESIN 600 MG 51674 0127

PHENYLEPHRINE 20 MG

120

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSE BPM LIQUID PSEUDOEPHEDRINE 60 MG 64376 0721 HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 4 MG

PSE CPM CHEWABLE TABLETS PSEUDOEPHEDRINE 15 MG 64376 0532 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

PSEUDO CHLOR SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 57866 0323

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

PSEUDO CMTR TABLETS CHLORPHENIRAMINE MALEATE 8 MG 64376 *032

METHSCOPOLAMINE NITRATE 2.5 MG

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

121

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDO COUGH SYRUP DEXTROMETHORPHAN 15 MG 64376 0733 HYDROBROMIDE

GUAIFENESIN 175 MG

PSEUDOEPHEDRINE 32 MG HYDROCHLORIDE

PSEUDO DM GG SYRUP PSEUDOEPHEDRINE 40 MG 64376 0712 HYDROCHLORIDE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

GUAIFENESIN 100 MG

PSEUDO GG TR EXTENDED GUAIFENESIN 595 MG 64376 *033 RELEASE TABLET

PSEUDOEPHEDRINE 48 MG HYDROCHLORIDE

122

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDO MAX DMX TABLETS DEXTROMETHORPHAN 40 MG 64376 *533 HYDROBROMIDE

GUAIFENESIN 700 MG

PSEUDOEPHEDRINE 80 MG HYDROCHLORIDE

PSEUDO MAX TABLETS GUAIFENESIN 700 MG 64376 *538

PSEUDOEPHEDRINE 80 MG HYDROCHLORIDE

PSEUDO/BROMPHEN MALEATE BROMPHENIRAMINE MALEATE 6 MG 54868 5491 TABLETS

PSEUDOEPHEDRINE 45 MG HYDROCHLORIDE

PSEUDOEPHEDRINE GG SYRUP GUAIFENESIN 200 MG 64376 0716

PSEUDOEPHEDRINE 40 MG HYDROCHLORIDE

123

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE GUAIFENESIN 1200 MG 66993 *332 HYDROCHLORIDE AND GUAIFENESIN EXTENDED RELEASE TABLETS PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

P-TEX BROMPHENIRAMINE TANNATE 10 50991 0927 MG/5ML

PULMARI GP SYRUP GUAIFENESIN 100 MG 60258 0425

CARBETAPENTANE CITRATE 20 MG

PYRLEX CB SUSPENSION PYRILAMINE TANNATE 12 MG 66813 162

CHLORPHENIRAMINE TANNATE 23 MG

PYRLEX PD SUSPENSION PHENYLEPHRINE TANNATE 9 MG 66813 0163

PYRILAMINE TANNATE 12 MG

124

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

Q BID DM TABLETS DEXTROMETHORPHAN 30 MG 00603 5541 HYDROBROMIDE

GUAIFENESIN 600 MG

Q BID DM TABLETS EXTENDED DEXTROMETHORPHAN 30 MG 00603 5542 RELEASE HYDROBROMIDE

GUAIFENESIN 600 MG

Q-BID LA TABLETS GUAIFENESIN 600 MG 00603 5543

QIUNTEX LIQUID GUAIFENESIN 100 MG 00603 1635

PHENYLEPHRINE 5 MG HYDROCHLORIDE

QUARTUSS DM DROPS PHENYLEPHRINE 1.5 MG 51991 0537 ANTITUSSIVE NASAL HYDROCHLORIDE DECONGESTANT ANTIHISTAMINE

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

125

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

CHLORPHENIRAMINE MALEATE 1 MG

QUARTUSS SYRUP DEXTROMETHORPHAN 15 MG 51991 0513 HYDROBROMIDE

GUAIFENESIN 100 MG

CHLORPHENIRAMINE MALEATE 2 MG

PENYLEPHRINE 10 MG HYDROCHLORIDE

RE DRYLEX JR EXTENDED CHLORPHENIRAMINE MALEATE 4 MG 68032 *212 RELEASE TABLET

METHSCOPOLAMINE NITRATE 1.25 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

RE DRYLEX SYRUP DEXCHLORPHENIRAMINE 1 MG 68032 0211 MALEATE

126

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

METHSCOPOLAMINE NITRATE 1.25 MG

RE PHENYLEPHRINE GUAIFENESIN 20 MG 68032 0368 GUAIFENESIN LIQUID

PHENYLEPHRINE 1.5 MG

RE ALLERGY AM/PM CHLORPHENIRAMINE MALEATE 8 MG 68032 0139

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

METHSCOPOLAMINE NITRATE 2.5 MG

REDUR PCM SUSPENSION PHENYLEPHRINE TANNATE 25 MG 68032 0207

CHLORPHENIRAMINE TANNATE 35 MG

127

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

RELCOF CPM TABLETS CHLORPHENIRAMINE MALEATE 8 MG 35573 *004

METHSCOPOLAMINE NITRATE 2.5 MG

RELCOF PE TABLETS CHLORPHENIRAMINE MALEATE 8 MG 35573 *003

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

RELCOF PSE TABLETS CHLORPHENIRAMINE MALEATE 8 MG 35573 *002

METHSCOPOLAMINE NITRATE 2.5 MG

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

REME HIST DM DEXTROMETHORPHAN 15 MG 68032 0192 HYDROBROMIDE

128

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 7.5 MG HYDROCHLORIDE

PYRILAMINE MALEATE 12.5 MG

REME TUSSIN DM COUGH CHLORPHENIRAMINE MALEATE 2 MG 68032 0191 SYRUP

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

PHENYLEPHRINE 5 MG HYDROCHLORIDE

RESCON BIPHASIC SUSTAINED CHLORPHENIRAMINE MALEATE 12 MG 64543 *096 RELEASE TABLETS

METHSCOPOLAMINE NITRATE 1.25 MG

PHENYLEPHRINE 40 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG 64543 *085

129

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

RESCON JR SUSTAINED RELEASE PHENYLEPHRINE 20 MG TABLETS HYDROCHLORIDE

RESCON MX SUSTAINED CHLORPHENIRAMINE MALEATE 8 MG 64543 *090 RELEASE TABLETS

METHSCOPOLAMINE NITRATE 2.5 MG

PHENYLEPHRINE 40 MG HYDROCHLORIDE

RESCON MX TABLETS DEXCHLORPHENIRAMINE 6 MG 64543 *091 SUSTAINED RELEASE RESCON- MALEATE ED CAPSULES

PHENYLEPHRINE 40 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 8 MG 11808 *089

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

RESPA 1ST TABLETS GUAIFENESIN 600 MG 60575 *087

130

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 58 MG HYDROCHLORIDE

RESPA BR TABLETS EXTENDED BROMPHENIRAMINE MALEATE 11 MG 60575 *786 RELEASE

RESPA DM TABLETS EXTENDED DEXTROMETHORPHAN 28 MG 60575 *078 RELEASE HYDROBROMIDE

GUAIFENESIN 600 MG

RESPA PE SUSTAINED RELEASE GUAIFENESIN 600 MG 60575 *787 TABLETS

PHENYLEPHRINE 18 MG HYDROCHLORIDE

RESPAHIST II EXTENDED BROMPHENIRAMINE MALEATE 6 MG 60575 *619 RELEASE TABLET

PHENYLEPHRINE 19 MG HYDROCHLORIDE

RESPAIRE 60 CAPSULE GUAIFENESIN 200 MG 00277 0174

131

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

RESPAIRE CAPSULES PSEUDOEPHEDRINE 30 MG 16477 0306 HYDROCHLORIDE

GUAIFENESIN 150 MG

RESPI TANN G SUSPENSION GUAIFENESIN 200 MG 67336 0188

CARBETAPENTANE CITRATE 7.5 MG

RESPIVENT D TABLETS METHSCOPOLAMINE NITRATE 2.5 MG 24486 *702 RESPIVENT DOSE PACK DF

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 8 MG 24486 0704

METHSCOPOLAMINE NITRATE 2.5 MG

132

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

RHINABID CAPSULES PHENYLEPHRINE 15 MG 51991 0092

BROMPHENIRAMINE 12 MG

RONDAMINE DM DROPS DEXTROMETHORPHAN 4 MG 00904 5573 HYDROBROMIDE

PSEUDOEPHEDRINE 15 MG HYDROCHLORIDE

RONDEC DM ORAL DROPS DEXTROMETHORPHAN 4 MG 64455 0050 HYDROBROMIDE

PSEUDOEPHEDRINE 15 MG HYDROCHLORIDE

RONDEC DM SYRUP DEXTROMETHORPHAN 15 MG 64455 0024 HYDROBROMIDE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

133

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

RONDEC SYRUP BROMPHENIRAMINE MALEATE 4 MG 64455 0061

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

RONDEC-DM DEXTROMETHORPHAN 4 MG/ML 64455 0023

PSEUDOEPHEDRINE 25 MG/ML

CARBINOXAMINE 2 MG/ML

RONDEC-DM DEXTROMETHORPHAN 4 MG/ML 64455 0070

PSEUDOEPHEDRINE 15 MG/ML

CARBINOXAMINE 1 MG/ML

RU TUSS DM SYRUP DEXTROMETHORPHAN 15 MG 15370 0006 HYDROBROMIDE

134

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 45 MG HYDROCHLORIDE

GUAIFENESIN 100 MG

RU TUSS DM SYRUP PSEUDOEPHEDRINE 45 MG 59243 0006 HYDROCHLORIDE

GUAIFENESIN 100 MG

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

RU TUSS DM TABLETS DEXTROMETHORPHAN 60 MG 59243 *012 HYDROBROMIDE

GUAIFENESIN 800 MG

RU TUSS JR TABLETS GUAIFENESIN 600 MG 59243 *017

PSEUDOEPHEDRINE 45 MG HYDROCHLORIDE

135

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

RY T 12 SUSPENSION SYRUP PHENYLEPHRINE TANNATE 5 MG 50383 0864

PYRILAMINE TANNATE 30 MG

RYNA 12 SUSPENSION RYNA 12 PHENYLEPHRINE TANNATE 5 MG 00037 0655 TABLETS

PYRILAMINE TANNATE 30 MG

PHENYLEPHRINE TANNATE 8 MG 00037 0673

PYRILAMINE TANNATE 27 MG

RYNA 12 X TABLETS GUAIFENESIN 200 MG 00037 1708

RYNA 12 X TABLETS PHENYLEPHRINE TANNATE 25 MG 00037 1708

PYRILAMINE TANNATE 60 MG

RYNEZE LIQUID GRAPE CHLORPHENIRAMINE MALEATE 4 MG 24839 0346

136

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

METHSCOPOLAMINE NITRATE 1.25 MG

SCOPOHIST PE TABLETS CHLORPHENIRAMINE MALEATE 8 MG 68047 *291

METHSCOPOLAMINE NITRATE 1.25 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

SCOPOHIST SYRUP METHSCOPOLAMINE NITRATE 0.75 MG 68047 0292

CHLORPHENIRAMINE MALEATE 2 MG

PHENYLEPHRINE 8 MG HYDROCHLORIDE

SCOPOHIST TABLETS CHLORPHENIRAMINE MALEATE 8 MG 68047 *290

METHSCOPOLAMINE NITRATE 1.25 MG

137

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

SERADEX LA TABLETS BROMPHENIRAMINE MALEATE 6 MG 28595 *110

PHENYLEPHRINE 19 MG HYDROCHLORIDE

SILDEC DM LIQUID DROPS DEXTROMETHORPHAN 4 MG 54838 0211 HYDROBROMIDE

PSEUDOEPHEDRINE 25 MG HYDROCHLORIDE

SILDEC DM ORAL DROPS DEXTROMETHORPHAN 4 MG 54838 0530 HYDROBROMIDE

PSEUDOEPHEDRINE 15 MG HYDROCHLORIDE

SILDEC DM ORAL DROPS PSEUDOEPHEDRINE 15 MG 54838 0537 HYDROCHLORIDE

138

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 4 MG HYDROBROMIDE

SILDEC DM SYRUP DEXTROMETHORPHAN 15 MG 54838 0212 HYDROBROMIDE

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

SILDEC PE DM SYRUP DEXTROMETHORPHAN 15 MG 54838 0544 HYDROBROMIDE

CHLORPHENIRAMINE MALEATE 4 MG

PHENYLEPHRINE 12.5 MG HYDROCHLORIDE

SILDEC PE SYRUP CHLORPHENIRAMINE MALEATE 4 MG 54838 0542

PHENYLEPHRINE 12.5 MG HYDROCHLORIDE

139

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

SIMUC DM ELIXIR DEXTROMETHORPHAN 25 MG 60258 0426 HYDROBROMIDE

GUAIFENESIN 225 MG

SINA 12X TABLETS PHENYLEPHRINE TANNATE 25 MG 00037 6301

SINUTUSS DM TABLETS PHENYLEPHRINE 15 MG 59196 0045 HYDROCHLORIDE

DEXTROMETHORPHAN 30 MG HYDROBROMIDE

GUAIFENESIN 600 MG

SINUVENT PE OMNIHIST LA ** ** 59196 0112

SINUVENT PE TABLETS PHENYLEPHRINE 15 MG 59196 0035 HYDROCHLORIDE

GUAIFENESIN 600 MG

140

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

SITREX PD LIQUID PHENYLEPHRINE 7.5 MG 67204 0042 HYDROCHLORIDE

GUAIFENESIN 75 MG

SITREX TABLETS GUAIFENESIN 1200 MG 67204 *064

PHENYLEPHRINE 30 MG HYDROCHLORIDE

SONAHIST DM PEDIATRIC PHENYLEPHRINE 2 MG 68032 0320 DROPS HYDROCHLORIDE

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

CHLORPHENIRAMINE MALEATE 1 MG

SONAHIST PEDIATRIC DROPS CHLORPHENIRAMINE MALEATE 1 MG 68032 0326

PHENYLEPHRINE 2 MG HYDROCHLORIDE

141

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

STAMOIST E EXTENDED GUAIFENESIN 500 MG 58407 0375 RELEASE TABLETS

PSEUDOEPHEDRINE 120 MG

STATUSS DM DEXTROMETHORPHAN 15 58407 0721 MG/5ML

PHENYLEPHRINE 10 MG/5ML

CHLORPHENIRAMINE 2 MG/5ML

SUCLOR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 62441 *200

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

SUDAHIST EXTENDED RELEASE CHLORPHENIRAMINE MALEATE 12 MG 68047 *330 TABLET

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

142

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

SUDATEX DM TABLETS PSEUDOEPHEDRINE 40 MG 68047 0242 HYDROCHLORIDE

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

GUAIFENESIN 400 MG

SUDATEX LIQUID PSEUDOEPHEDRINE 40 MG 68047 0124 HYDROCHLORIDE

GUAIFENESIN 200 MG

SUDATRATE TABLETS METHSCOPOLAMINE NITRATE 2.5 MG 68047 *245

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

SYMPAK PDX CHLORPHENIRAMINE 2 MG 59196 0119

PHENYLEPHRINE 10 MG

143

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

METHSCOPOLAMINE 1.5 MG

SYMPAK SINUTUSS AND DEXTROMETHORPHAN 30 MG 59196 *120 OMNIHIST II HYDROBROMIDE

PHENYLEPHRINE 15 MG HYDROCHLORIDE

GUAIFENESIN 600 MG

TANA R-12 PHENYLEPHRINE 5 MG/5ML 66239 0180

PYRILAMINE TANNATE 30 MG/5ML

TANABID CHEWABLE CAPLETS BROMPHENIRAMINE 2.2 MG 49963 0610

PHENYLEPHRINE 1.58 MG

TANACOF XR ANTIHISTAMINE BROMPHENIRAMINE TANNATE 12 MG 68047 0142 FOR SUSPENSION

144

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

TANACOF XR ANTIHISTAMINE BROMPHENIRAMINE TANNATE 8 MG 68047 0142 FOR SUSPENSION

TANAHIST PD PEDIATRIC DROPS CHLORPHENIRAMINE TANNATE 2 MG 68047 0030 SUSPENSION

TANNATE 12D S CARBETAPENTANE 30 MG/ML 50383 0841

PHENYLEPHRINE 5 MG/ML

PYRILAMINE 30 MG/ML

TENAR DM SYRUP GUAIFENESIN 200 MG 11528 0120

PSEUDOEPHEDRINE 32 MG HYDROCHLORIDE

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

TENAR PSE LIQUID GUAIFENESIN 200 MG 11528 0115

145

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 40 MG HYDROCHLORIDE

TIME HIST QD TABLETS CHLORPHENIRAMINE MALEATE 6 MG 66870 *701

METHSCOPOLAMINE NITRATE 2.5 MG

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

TOURO CC CAPLETS DEXTROMETHORPHAN 30 MG 58869 *441 HYDROBROMIDE

GUAIFENESIN 575 MG

PSEUDOEPHEDRINE 60 MG HYDROCHLORIDE

TOURO CC LD CAPLEST DEXTROMETHORPHAN 30 MG 58869 *445 HYDROBROMIDE

GUAIFENESIN 575 MG

146

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 25 MG HYDROCHLORIDE

TOURO DM TABLETS DEXTROMETHORPHAN 30 MG 58869 *411 HYDRIODIDE

GUAIFENESIN 575 MG

TOURO LA LD CAPLETS GUAIFENESIN 525 MG 58869 *635

PSEUDOEPHEDRINE 50 MG HYDROCHLORIDE

TOURO LA TABLETS GUAIFENESIN 525 MG 58869 *636

PSEUDOEPHEDRINE 120 MG HYDROCHLORIDE

TRIALL SYRUP PHENYLEPHRINE 8 MG 51991 0524 HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 2 MG

147

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

METHSCOPOLAMINE NITRATE 0.75 MG

TRIKOF D EXTENDED RELEASE DEXTROMETHORPHAN 30 MG 60575 *457 TABLET HYDROBROMIDE

GUAIFENESIN 600 MG

PSEUDOEPHEDRINE 50 MG HYDROCHLORIDE

TRIPLEX DM LIQUID PHENYLEPHRINE 7.5 MG 51991 0493 HYDROCHLORIDE

PYRILAMINE MALEATE 12.5 MG

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

TRISPEC DMX LIQUID CHERRY GUAIFENESIN 25 MG 58238 0211

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

148

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

TRISPEC DMX PEDIATRIC DROPS DEXTROMETHORPHAN 15 MG 58238 0212 CHERRY HYDROBROMIDE

GUAIFENESIN 25 MG

TRISPEC PSE LIQUID GRAPE DEXTROMETHORPHAN 15 MG 58238 0213 HYDROBROMIDE

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

GUAIFENESIN 25 MG

TRISPEC PSE PEDIATRIC DROPS DEXTROMETHORPHAN 15 MG 58238 0214 GRAPE HYDROBROMIDE

GUAIFENESIN 25 MG

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

149

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

TRITAL DM LIQUID DEXTROMETHORPHAN 15 MG 51991 0131 HYDROBROMIDE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

CHLORPHENIRAMINE MALEATE 4 MG

TRITUSS ER CAPLETS DEXTROMETHORPHAN 30 MG 00642 0661 HYDROBROMIDE

GUAIFENESIN 600 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

TRITUSS SYRUP DEXTROMETHORPHAN 25 MG 00642 0700 HYDROBROMIDE

GUAIFENESIN 175 MG

150

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 12.5 MG HYDROCHLORIDE

TUSDEC DM LIQUID DEXTROMETHORPHAN 15 MG 60258 0431 HYDROBROMIDE

PHENYLEPHRINE 7.5 MG HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 2 MG

TUSNEL GUAIFENESIN 200 MG 54859 0801

DEXTROMETHORPHAN 15 MG

BROMPHENIRAMINE 2 MG

TUSNEL PEDIATRIC COUGH GUAIFENESIN 50 MG 54859 0544 SYRUP

PSEUDOEPHEDRINE 15 MG HYDROCHLORIDE

151

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 5 MG HYDROBROMIDE

TUSNEL PEDIATRIC DROPS GUAIFENESIN 50 MG 54859 0602

PSEUDOEPHEDRINE 5 MG HYDROCHLORIDE

TUSNEL SYRUP GUAIFENESIN 200 MG 54859 0502

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

BROMPHENIRAMINE MALEATE 2 MG

TUSNEL-DM GUAIFENESIN 25 MG/ML 54859 0603

DEXTROMETHORPHAN 5 MG/ML

PSEUDOEPHEDRINE 5 MG/ML

152

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

TUSSAFED EX LIQUID DEXTROMETHORPHAN 30 MG 53879 0103 HYDROBROMIDE

GUAIFENESIN 200 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

TUSSAFED EX SYRUP PHENYLEPHRINE 10 MG 00642 0765 HYDROCHLORIDE

DEXTROMETHORPHAN 30 MG HYDROBROMIDE

GUAIFENESIN 200 MG

TUSSAFED LA CAPLETS GUAIFENESIN 600 MG 00642 0650

DEXTROMETHORPHAN 30 MG

PSEUDOEPHEDRINE 60 MG

153

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

TUSSBID CAPSULES GUAIFENESIN 400 MG 51991 0088

PHENYLEPHRINE 15 MG

TUSSI 12 D TABLETS PHENYLEPHRINE TANNATE 10 MG 00037 0692

CARBETAPENTANE TANNATE 60 MG

PYRILAMINE TANNATE 40 MG

TUSSI 12D S SUSPENSION PYRILAMINE TANNATE 30 MG 00037 0693

PHENYLEPHRINE TANNATE 5 MG

CARBETAPENTANE TANNATE 30 MG

TUSSI PRES SYRUP DEXTROMETHORPHAN 15 MG 52083 0233 HYDROBROMIDE

GUAIFENESIN 200 MG

154

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

TUSSIDEX LIQUID GRAPE PHENYLEPHRINE 10 MG 64320 0729 FLAVOR HYDROCHLORIDE

GUAIFENESIN 200 MG

DEXTROMETHORPHAN 30 MG HYDROBROMIDE

TUSSO DM CAPLETS DEXTROMETHORPHAN 23 MG 00642 0630 HYDROBROMIDE

GUAIFENESIN 600 MG

PHENYLEPHRINE 9 MG HYDROCHLORIDE

TUSSO DMR CAPSULES GUAIFENESIN 288 MG 00642 0645

155

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

DEXTROMETHORPHAN 7 MG HYDROBROMIDE

TUSSO ZMR CAPSULES GUAIFENESIN 200 MG 00642 0647

CARBETAPENTANE CITRATE 8 MG

TUSSO ZR SYRUP CARBETAPENTANE CITRATE 7.5 MG 00642 0649

GUAIFENESIN 150 MG

V TAN DM GRAPE FLAVORED DEXTROMETHORPHAN 25 MG 50383 0856 SUSPENSION TANNATE

PYRILAMINE TANNATE 30 MG

PHENYLEPHRINE TANNATE 12.5 MG

V TANN TABLETS CHEWABLE PYRILAMINE TANNATE 30 MG 51991 0267

156

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE TANNATE 25 MG

VANACOF CD PHENYLEPHRINE 5 MG 58809 0817

DEXCHLORPHENIRAMINE 1 MG MALEATE

VAZOBID TANNATE PHENYLEPHRINE 10 ML 66992 0230 SUSPENSION HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 6 ML

VAZOL D LIQUID PHENYLEPHRINE 7.5 MG 66992 0136 HYDROCHLORIDE

BROMPHENIRAMINE MALEATE 4 MG

VIRATAN DM CHEWABLE PHENYLEPHRINE TANNATE 25 MG 62559 5742 TABLETS

DEXTROMETHORPHAN 25 MG TANNATE

157

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PYRILAMINE TANNATE 30 MG

VIRATAN DM SUSPENSION PYRILAMINE TANNATE 30 MG 62559 5741

PHENYLEPHRINE TANNATE 12.5 MG

DEXTROMETHORPHAN 25 MG TANNATE

VIRAVAN DM DEXTROMETHORPHAN 25 MG 66346 0142

PHENYLEPHRINE 25 MG

PYRILAMINE 30 MG

VIRAVAN P TANNATE PSEUDOEPHEDRINE 15 MG 23589 0011 SUSPENSION CHERRY HYDROCHLORIDE BUBBLEGUM FLAVORED

PYRILAMINE MALEATE 15 MG

158

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

VIRAVAN PDM GRAPE PSEUDOEPHEDRINE 15 MG 23589 0013 FLAVORED TANNATE HYDROCHLORIDE SUSPENSION

PYRILAMINE MALEATE 15 MG

DEXTROMETHORPHAN 15 MG HYDROBROMIDE

VIRAVAN T GRAPE FLAVORED PYRILAMINE TANNATE 30 MG 66346 0032 TABLETS

PHENYLEPHRINE TANNATE 25 MG

VISONEX TABLETS SUSTAINED GUAIFENESIN 900 MG 68013 *009 RELEASE

PHENYLEPHRINE 30 MG

VISRX DOSE PACK TABLETS METHSCOPOLAMINE NITRATE 2.5 MG 68013 0014

CHLORPHENIRAMINE MALEATE 8 MG

159

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

WE ALLERGY CHLORPHENIRAMINE MALEATE 2 MG 59196 0070

METHSCOPOLAMINE NITRATE 0.625 MG

PHENYLEPHRINE 10 MG HYDROCHLORIDE

WELLBID D 1200 SUSTAINED GUAIFENESIN 1200 MG 66993 *316 RELEASE TABLETS

PHENYLEPHRINE 40 MG HYDROCHLORIDE

WELLBID D SUSTAINED RELEASE GUAIFENESIN 600 MG 66993 *315 TABLETS

PHENYLEPHRINE 40 MG HYDROCHLORIDE

Z COF 8DM DEXTROMETHORPHAN 15 MG 65224 0616 HYDROBROMIDE

GUAIFENESIN 175 MG

160

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PSEUDOEPHEDRINE 30 MG HYDROCHLORIDE

Z COF LA TABLETS DEXTROMETHORPHAN 30 MG 65224 *105 HYDROCHLORIDE

GUAIFENESIN 650 MG

Z DEX 12D TABLETS DEXTROMETHORPHAN 30 MG 13811 *003 HYDROCHLORIDE

PHENYLEPHRINE 20 MG HYDROCHLORIDE

CHLORPHENIRAMINE 8 MG HYDROCHLORIDE

Z DEX PEDIATRIC DROPS PHENYLEPHRINE 2.5 MG 13811 0001 HYDROCHLORIDE

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

161

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

GUAIFENESIN 35 MG

Z DEX SYRUP GUAIFENESIN 100 MG 13811 0002

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

PHENYLEPHRINE 10 MG HYDROCHLORIDE

ZOTEX 12 SUSPENSION DEXTROMETHORPHAN 2.5 MG 68025 0024 TANNATE

PHENYLEPHRINE TANNATE 15.5 MG

PYRILAMINE TANNATE 15.5 MG

ZOTEX 12D SUSTAINED RELEASE DEXTROMETHORPHAN 30 MG 68025 *033 TABLETS HYDROCHLORIDE

CHLORPHENIRAMINE 8 MG HYDROCHLORIDE

162

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

PHENYLEPHRINE 20 MG HYDROCHLORIDE

ZOTEX GP CAPLETS GUAIFENESIN 550 MG 68025 0005

PHENYLEPHRINE 8.5 MG HYDROCHLORIDE

ZOTEX GPX CAPLETS GUAIFENESIN 550 MG 68025 *020 EXPECTORANT

PHENYLEPHRINE 8.5 MG HYDROCHLORIDE

ZOTEX LA CAPLETS DEXTROMETHORPHAN 25 MG 68025 *002 HYDROBROMIDE

GUAIFENESIN 500 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

163

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

ZOTEX LAX CAPLETS DEXTROMETHORPHAN 25 MG 68025 *018 HYDROBROMIDE

GUAIFENESIN 550 MG

PHENYLEPHRINE 20 MG HYDROCHLORIDE

ZOTEX PE SUSTAINED RELEASE BROMPHENIRAMINE MALEATE 6 MG 68025 *034 TABLETS

PHENYLEPHRINE 30 MG HYDROCHLORIDE

ZOTEX PEDIATRIC DROPS PHENYLEPHRINE 2.5 MG 68025 0003 HYDROCHLORIDE

DEXTROMETHORPHAN 3 MG HYDROBROMIDE

GUAIFENESIN 35 MG

164

SINthetic Pharmaceutical = ‘Poison of the Witch’

NDC NDC LABELER PRODUCT NAME OF DRUG INGREDIENTS STRENGTH CODE CODE

ZOTEX SYRUP PHENYLEPHRINE 10 MG 68025 0001 HYDROCHLORIDE

DEXTROMETHORPHAN 20 MG HYDROBROMIDE

GUAIFENESIN 100 MG

ZYMINE DRX SUSPENSION PSEUDOEPHEDRINE TANNATE 45 MG 67204 0340

TRIPROLIDINE TANNATE 2.5 MG

ZYMINE XR SUSPENSION TRIPROLIDINE TANNATE 2.5 MG 67204 0325

See also

 Adverse drug reaction  Adverse events (AEs)  European Medicines Agency  Food and Drug Administration

165

SINthetic Pharmaceutical = ‘Poison of the Witch’ References

1. Health Canada press release 2. ^ to:a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae Qureshi, ZP; Seoane-Vazquez, E; Rodriguez- Monguio, R; Stevenson, KB; Szeinbach, SL (July 2011). "Market withdrawal of new molecular entities approved in the United States from 1980 to 2009.". Pharmacoepidemiology and drug safety 20 (7): 772–7. doi:10.1002/pds.2155. PMID 21574210. 3. ^ to:a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx bybz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg d h di dj dk Fung, M.; Thornton, A.; Mybeck, K.; Wu, J. H.-h.; Hornbuckle, K.; Muniz, E. (1 January 2001). "Evaluation of the Characteristics of Safety Withdrawal of Prescription Drugs from Worldwide Pharmaceutical Markets-1960 to 1999". Therapeutic Innovation & Regulatory Science 35 (1): 293– 317. doi:10.1177/009286150103500134. 4. WHO Drug Information Vol. 8, No. 2, 1994, page 64 5. Berson A, et al. (2001) Toxicity of alpidem, a peripheral benzodiazepine receptor ligand, but not zolpidem, in rat hepatocytes: role of mitochondrial permeability transition and metabolic activation. J Pharmacol Exp Ther. 299(2):793-800. 6. DrugBank. "". Retrieved 24 September 2013. 7. FDA Response to Citizen Request re Ardeparin 8. DrugBank. "Bezitramide". Retrieved 24 September 2013. 9. DrugBank. "Bunamiodyl". Retrieved 24 September 2013. 10. Department of Economic and Social Affairs of the United Nations Secretariat Consolidated List of Products Whose Consumption and/or Sale Have Been Banned, Withdrawn, Severely Restricted or not Approved by Governments Twelfth Issue: Pharmaceuticals United Nations – New York, 2005 11. ^ to:a b c d e f g Schubert-Zsilavecz, Manfred (2011). "Arzneimittelrücknahmen Rückrufe im Rückblick". Pharmazeutische Zeitung (German). Retrieved 25 September 2013. 12. DrugBank. "Dantron". Retrieved 24 September 2013. 13. FDA announcement 14. ^ to:a b Col John Lammie et al. Report of the Department Of Defense: 1,3 Dimethylamylamine (Dmaa) Safety Review Panel June 3, 2013 15. FDA. " Potentially Dangerous to Health, FDA Warns". Retrieved 26 January 2014. 16. Drotrecogin Alfa (Activated) in Adults with Septic Shock , N Engl J Med 2012; 366:2055-2064, May 31, 2012, DOI: 10.1056/NEJMoa1202290 17. "Xigris (drotrecogin alfa (activated)) to be withdrawn due to lack of efficacy". Press release. London, UK: European Medicines Agency. 25 October 2011. Archived from the original on 26 October 2011. Retrieved 26 October 2011. 18. http://www.businessweek.com/news/2011-10-25/lilly-pulls-xigris-off-markets-after-sepsis-drug-fails- study.html 19. DrugBank. "Ethyl carbamate". Retrieved 24 September 2013. 20. DrugBank. "Fenfluramine". Retrieved 24 September 2013. 21. DrugBank. "Iproniazid". Retrieved 24 September 2013. 22. Centers for Disease Control and Prevention (CDC) (December 2009). "Agranulocytosis associated with use - four States, March 2008-November 2009". Morb. Mortal. Wkly. Rep. 58 (49): 1381– 5. PMID 20019655. 23. Nancy Y Zhu; Donald F. LeGatt; A Robert Turner (February 2009). "Agranulocytosis After Consumption of Cocaine Adulterated With Levamisole". Annals of Internal Medicine150 (4): 287– 289. doi:10.1059/0003-4819-150-4-200902170-00102. PMID 19153405. Retrieved 2009-10-07. 24. Kinzie, Erik (April 2009). "Levamisole Found in Patients Using Cocaine". Annals of Emergency Medicine 53 (4): 546–7. doi:10.1016/j.annemergmed.2008.10.017.PMID 19303517. Retrieved 2009- 08-18. 25. Central Drugs Standard Control Organization. "Drugs Banned In India". Ministry of Health and Family Welfare, Government of India. Retrieved 24 September 2013. 26. "Drug Effects - Methaqualone". South African Police Service. Retrieved 24 September 2013. 27. Cosgrove-Mather, Bootie (December 5, 2007). "Anti-Depressant Taken Off Market". CBS NEWS. Retrieved 29 September 2013.

166

SINthetic Pharmaceutical = ‘Poison of the Witch’

28. DrugBank. "Oxeladin". Retrieved 24 September 2013. 29. DrugBank. "Oxyphenbutazone". Retrieved 24 September 2013. 30. DrugBank. "Pemoline". Retrieved 24 September 2013. 31. DrugBank. "Phenacetin". Retrieved 24 September 2013. 32. Wysowski, Diane K. (2005). "Adverse Drug Event Surveillance and Drug Withdrawals in the United States, 1969-2002The Importance of Reporting Suspected Reactions". Archives of Internal Medicine 165 (12): 1363– 9. doi:10.1001/archinte.165.12.1363. PMID 15983284. |first2= missing |last2= in Authors list (help) 33. FDA Advisory 34. DrugBank. "". Retrieved 24 September 2013. 35. WHO. Consolidated List of Products - Whose Consumption and/or Sale Have Been Banned, Withdrawn, Severely Restricted or Not Approved by Governments, Twelfth Issue - Pharmaceuticals. United Nations - New York, 2005 36. DrugBank. "". Retrieved 24 September 2013. 37. DrugBank. "". Retrieved 24 September 2013. 38. "Sibutramine (brand name Reductil) Information - Australia". Abbott Laboratories. 2010. Retrieved 2010-10-08. 39. Health Canada Endorsed Important Safety Information on MERIDIA (Sibutramine Hydrochloride Monohydrate): Subject: Voluntary withdrawal of Meridia (sibutramine) capsules from the Canadian market. 40. "Notification of Termination of Production, Sale, and Usage of Sibutramine Preparations and Their Active Pharmaceutical Ingredient". sda.gov in People's Republic of China. October 30, 2010. Retrieved 2011-05-21. 41. (German) Sibutramin-Vertrieb in der Europäischen Union ausgesetzt [1]. Abbott Laboratories in Germany. Press Release 2010-01-21. Retrieved 2010-01-27 42. "De-registration of pharmaceutical products containing sibutramine" (Press release). info.gov in Hong Kong. November 2, 2010. Retrieved 2010-11-08. 43. "Banned Medicines" (Press release). Ministry of Health and Family Welfare. February 10, 2011. Retrieved 2011-03-15. 44. "Withdrawal of Sibutramine (Reductil) in New Zealand" (Press release). MedSafe in New Zealand. October 11, 2010. Retrieved 2012-11-06. 45. "FDA warns online sellers of banned slimming pills". January 12, 2014. Retrieved February 20, 2014. 46. "Thai FDA reveals voluntary withdrawal of sibutramine from the Thai market" (PDF) (Press release). Food and Drug Administration of Thailand. October 20, 2010. Retrieved2010-12-22. 47. "Top obesity drug sibutramine being suspended". BBC News. 2010-01-22. Retrieved 2010-01-22. 48. Rockoff, Jonathan D.; Dooren, Jennifer Corbett (October 8, 2010). "Abbott Pulls Diet Drug Meridia Off US Shelves". The Wall Street Journal. Retrieved 8 October 2010. 49. H. Gurdon: Japan bans shingles drug after deaths BMJ 1994;309:627 50. Paar, W.D; Müller-Jakic. "Ruhen der Zulassung Tetrazepam haltiger Arzneimittel in der EU (German)" (PDF). Sanofi-Aventis Deutschland GmbH. Retrieved 25 September2013. 51. Luippold, Gerd (2006). "Renaissance des Contergan-Wirkstoffs". Pharmazeutische Zeitung (German). Retrieved 25 September 2013. 52. Drugbank. "Thenalidine". Retrieved 24 September 2013. 53. Purhonen, M; Koponen, H; Tiihonen, J; Tanskanen, A (November 2012). "Outcome of patients after market withdrawal of thioridazine: A retrospective analysis in a nationwide cohort". Pharmacoepidemiology and Drug Safety 21 (11): 1227– 1231. doi:10.1002/pds.3346. PMID 22941581. 54. "SHARED CARE PROTOCOL Thioridazine" (PDF). NHS Lothian Joint Formulary. March 2012. 55. DrugBank. "Triazolam". Retrieved 24 September 2013. 56. Fagius J, et al. Guillain-Barré syndrome following zimeldine treatment J Neurol Neurosurg Psychiatry. 1985 Jan;48(1):65-9. 57. Pubchem record says "withdrawn in 1983" 58. DrugBank. "Zimelidine". Retrieved 24 September 2013.

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168

SINthetic Pharmaceutical = ‘Poison of the Witch’

169