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Marketed as a psychiatric 1950 drug; withdrawn after it Lysergic acid s– became widely used diethylamide (LSD) 1960 recreationally.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 tyrosine.[22]
Unspecific experimental
Metofoline 1965 US toxicity.[3]
[3] Pronethalol 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] Chlorphentermine 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] Pyrovalerone 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-tryptophan 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] Dexfenfluramine 1997 European Union, UK, US Cardiac valvular disease.
Fen-phen (popular combination of fenfluramine 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. Pemoline (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 Alosetron (Lotronex) 2000 US constipation.[2] Reintroduced 2002 on a restricted basis[citation needed]
Risk of fatal cardiac Cisapride (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 Adderall 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 alcohol. 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 Thioridazine (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 Nefazodone 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 Pergolide (Permax) 2007 US damage.[2]
Risk for heart attack, stroke, and unstable angina.[2] Was Tegaserod (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 Rimonabant (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 Sibutramine (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 DIPHENHYDRAMINE 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 CYPROHEPTADINE 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 ANTIHISTAMINE & 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-EPHEDRINE-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. "Amineptine". 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. "Stimulant 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 cocaine 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.
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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, 1969-2002
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SINthetic Pharmaceutical = ‘Poison of the Witch’
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