Merck Succumbs to Urge to Mega-Merge

Total Page:16

File Type:pdf, Size:1020Kb

Merck Succumbs to Urge to Mega-Merge March 09, 2009 Merck succumbs to urge to mega-merge Evaluate Vantage Since Pfizer made a somewhat desperate move in January to try and retain its number one ranking as the industry’s biggest pharmaceutical company by acquiring Wyeth for $68bn (Pfizer’s desperate move on Wyeth, January 26, 2009), the fear has been that this would trigger a new wave of mega-merger consolidation; good news for banks, consultants and lawyers but ultimately bad news for shareholders as short-term cost savings rarely translate into long-term value. Today’s revelation that Merck & Co is acquiring Schering-Plough for $41.1bn at a 34% premium, through a complicated “reverse-merger” deal designed to try and retain rights to key products, indicates a new mega- merger wave is upon us. Whilst Pfizer’s move for Wyeth was not surprising given its mega-merger history, Merck’s bid for Schering marks a significant change in strategy. Previously the group’s biggest company acquisition was a $1.1bn swoop on Sirna Therapeutics in 2006, suggesting the industry’s patent cliff is causing desperate companies to adopt desperate measures. Climbing the league In terms of the global league table for pharmaceutical sales, the Merck-Schering tie up would certainly propel both companies up the rankings, with combined sales in 2008 of $41.3bn set to grow 2% annually to $45.3bn by 2014. This ranks the new company in third position, behind the Pfizer+Wyeth merged company and Roche. The table below, which uses EvaluatePharma’s merge companies tool to create a virtual merged company, Merck+Schering-Plough, shows the top ten companies by pharmaceutical sales in 2014 and reflects a rapidly changing landscape for the industry’s leading companies. WW pharmaceutical rankings in Prescription (Rx) sales Market Market 2014 ($m) Share Rank CAGR (08 - 2008 2014 2008 2014 2008 2014 14) Pfizer+Wyeth 57,682 48,200 (3%) 9.4% 6.6% 1 1 Roche 33,277 47,721 6% 5.4% 6.5% 6 2 Merck+Schering-Plough 41,296 45,284 2% 6.7% 6.2% 3 3 Novartis 34,462 45,074 5% 5.6% 6.1% 5 4 Sanofi-Aventis 41,444 37,128 (2%) 6.7% 5.0% 2 5 GlaxoSmithKline 36,890 33,180 (2%) 6.0% 4.5% 4 6 Pfizer 41,923 29,344 (6%) 6.8% 4.0% - - Johnson & Johnson 23,510 25,880 2% 3.8% 3.5% 8 7 Merck & Co 25,256 25,537 0% 4.1% 3.5% - - Abbott Laboratories 17,174 22,672 5% 2.8% 3.1% 10 8 AstraZeneca 30,264 21,806 (5%) 4.9% 3.0% 7 9 Schering-Plough 16,040 19,747 4% 2.6% 2.7% - - Wyeth 15,759 18,857 3% 2.6% 2.6% - - Teva Pharmaceutical Industries 9,538 18,848 12% 1.6% 2.6% 16 10 Although a slight aside, perhaps one of the most intriguing aspects of this changing landscape is the appearance in this top ten league of the world’s leading generics company, Teva Pharmaceutical Industries. Reverse merger trend Although there is a recent trend for increasing numbers of reverse mergers, these normally involve a small- sized private company backing into a distressed public company. The reverse merger terms of this deal, with Schering-Plough effectively the surviving entity but Merck’s shareholders controlling 68% of the combined company, was therefore something of a surprise. The rationale for such a complicated move appears to be designed to avoid triggering a change of control clause over Schering’s key rheumatoid arthritis antibodies, Remicade and golimumab, licensed from Johnson & Johnson’s biotech subsidiary Centocor. Schering holds commercialisation rights to both products outside the US. Remicade was Schering’s biggest selling drug last year with sales of $2.1bn and is the group’s most valuable product with an NPV of $4.58bn, according to EvaluatePharma’s NPV Analyzer. Meanwhile, golimumab, currently under review in both the US and Europe and with a proposed trade name of Simponi, is Schering’s biggest revenue growth driver over the next six years, with international sales of $902m by 2014. With so much riding on the value of these products, the company was keen to stress it believes the merger structure is such that on a technical level Schering is still the surviving company. Whether J&J will accept such an argument remains to be seen and it can be assumed they will be looking closely at the terms and conditions of the original license and assessing whether they want to pursue legal avenues to try and acquire both products outright. Patent cliff bites Whilst most big pharma companies are still facing a precipitous patent cliff, Merck is already sliding rapidly down its own. The group’s top three biggest-selling products in 2007, Singulair, Cozaar and Fosamax with combined sales of $10.7bn, are all set to be exposed to generic competition by 2012. Fosamax’s patent expired last year, Cozaar goes generic in 2010 and Singulair’s patent, currently being challenged by Teva (Merck set for Singulair patent battle, February 16, 2009) will expire in 2012, or earlier if Teva prevails or a compromise is reached. In a similar vein to Pfizer, which prior to the Wyeth deal talked up the prospects of smaller, more manageable acquisitions to drive long-term growth, it appears Merck’s current situation has also caused a change of heart, having previously made strong noises about seeking medium-sized acquisitions (Who might be on Merck's shopping list?,May 2, 2008). Right transaction, right time A consistent message from the company’s conference call, particularly from Schering’s chief executive officer, Fred Hassan, who previously sold Pharmacia to Pfizer in 2003, was of this tie up between Merck and Schering being the “right transaction, at the right time”. Both companies have been severely hit by the decline in current sales and prospects for two lipid-lowering agents, Vytorin and Zetia, the commercialisation of which is conducted by their joint venture, Merck/Schering- Plough JV. Schering’s market capitalisation, before this deal, of $28.7bn is significantly lower than the sum of the group’s NPV of marketed products at $36.9bn. Although Merck’s offer of $23.61 per share, split 44% in cash and 56% in stock, is a 34% premium to Schering’s share price of $17.63 on March 6, compared to the valuation of the group’s future cash flows even just for marketed products, the premium is a lot lower at 11%. Merck is therefore virtually getting Schering’s pipeline, currently valued at $11.5bn, for free. Despite the potential bargain of this deal, Merck’s shareholders seem unimpressed, sending shares in the group down 10% today to $20.59, a 14-year low. It therefore appears shareholders are subscribing to the view that these mega-mergers tend only to erode value and have not been swayed by the cost-saving and synergy arguments put forward by senior management of both companies. More from Evaluate Vantage Evaluate HQ 44-(0)20-7377-0800 Evaluate Americas +1-617-573-9450 Evaluate APAC +81-(0)80-1164-4754 © Copyright 2021 Evaluate Ltd..
Recommended publications
  • Print Layout 1
    TECHNICAL PROGRAM Monday, March 19 5:00 – 8:00 pm Welcome Reception Tuesday, March 20 8:00 – 10:00 Session 1: Setting the Conference Context and Drivers Chair: Geoff Slaff (Amgen) Roger Perlmutter (Amgen) Conquering the Innovation Deficit in Drug Discovery Helen Winkle (CDER, FDA) Regulatory Modernization 10:00 – 10:30 Break Vendor and poster review 10:30 – 12:30 Session 2: Rapid Cell Line Development and Improved Expression System Development Chairs: Timothy Charlebois (Wyeth) and John Joly (Genentech) Amy Shen (Genentech) Stable Antibody Production Cell-Line Development with an Improved Selection Process and Accelerated Timeline Mark Leonard (Wyeth) High-Performing Cell-Line Development within a Rapid and Integrated Platform Process Control Pranhitha Reddy (Amgen) Applying Quality-by-Design to Cell Line Development Lin Zhang (Pfizer) Development of a Fully-Integrated Automated System for High-Throughput Screening and Selection of Single Cells Expressing Monoclonal Antibodies 12:30 – 2:00 Lunch Vendor and poster review 2:00 – 4:30 Session 3: High-Throughput Bulk Process Development Chairs: Brian Kelley (Wyeth) and Jorg Thommes (Biogen Idec) Colette Ranucci (Merck) Development of a Multi-Well Plate System for High-Throughput Process Development Min Zhang (SAFC Biosciences) CHO Media Library – an Efficient Platform for Rapid Development and Optimization of Cell Culture Media Supporting High Production of Pharmaceutical Proteins in Chinese Hamster Ovary Cells Nigel Titchener-Hooker The Use of Ultra-Scale-Down Approaches to Enable Rapid Investigation
    [Show full text]
  • Moderna Vaccine Day Presentation
    Zika Encoded VLP mRNA(s) RSV CMV + EBV SARS-CoV- RSV-ped 2 Flu hMPV/PIV3 H7N9 Encoded mRNA(s) Ribosome Protein chain(s) First Vaccines Day April 14, 2020 © 2020 M oderna Therapeutics Forward-looking statements and disclaimers This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended including, but not limited to, statements concerning; the impact of the SARS-CoV-2 pandemic on the Company’s clinical trials and operations; the timing and finalization of a dose-confirmation Phase 2 study and planning for a pivotal Phase 3 study for mRNA-1647; the status and outcome of the Phase 1 clinical trial for mRNA-1273 being conducted by NIH; the next steps and ultimate commercial plan for mRNA-1273; the size of the potential market opportunity for mRNA-1273; the size of the potential commercial market for novel vaccines produced by Moderna or others; the potential peak sales for the Company’s wholly-owned vaccines; the probability of success of the Company’s vaccines individually and as a portfolio; and the ability of the Company to accelerate the research and development timeline for any individual product or the platform as a whole. In some cases, forward-looking statements can be identified by terminology such as “will,” “may,” “should,” “expects,” “intends,” “plans,” “aims,” “anticipates,” “believes,” “estimates,” “predicts,” “potential,” “continue,” or the negative of these terms or other comparable terminology, although not all forward-looking statements contain these words. The forward-looking statements in this press release are neither promises nor guarantees, and you should not place undue reliance on these forward-looking statements because they involve known and unknown risks, uncertainties, and other factors, many of which are beyond Moderna’s control and which could cause actual results to differ materially from those expressed or implied by these forward-looking statements.
    [Show full text]
  • Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc Mylotarg
    Mylotarg FDA ODAC Briefing Document 11 July 2017 WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC MYLOTARG (gemtuzumab ozogamicin; PF-05208747) In combination with chemotherapy for the treatment of previously untreated de novo CD33-positive acute myeloid leukemia and as monotherapy for the treatment of CD33-positive acute myeloid leukemia in first relapse FDA ONCOLOGIC DRUGS ADVISORY COMMITTEE BRIEFING DOCUMENT (BLA 761060) Meeting Date: 11 July 2017 ADVISORY COMMITTEE BRIEFING MATERIALS: AVAILABLE FOR PUBLIC RELEASE 090177e18c1aa788\Approved\Approved On: 12-Jun-2017 13:05 (GMT) Page 1 Mylotarg FDA ODAC Briefing Document 11 July 2017 TABLE OF CONTENTS TABLE OF CONTENTS...........................................................................................................2 LIST OF TABLES.....................................................................................................................5 LIST OF FIGURES ...................................................................................................................6 1. EXECUTIVE SUMMARY .................................................................................................7 1.1. Introduction..............................................................................................................7 1.2. Rationale for Mylotarg Dosing Regimens ...............................................................8 1.3. Mylotarg in Patients With Previously Untreated De Novo AML............................9 1.4. Mylotarg in Patients With AML in First Relapse..................................................11
    [Show full text]
  • Amgen and Wyeth Statement on FDA Announcement About Tumor Necrosis Factor (TNF) Blockers
    Amgen and Wyeth Statement on FDA Announcement About Tumor Necrosis Factor (TNF) Blockers August 4, 2009 THOUSAND OAKS, Calif. and COLLEGEVILLE, Pa., Aug. 4 /PRNewswire-FirstCall/ -- Amgen (Nasdaq: AMGN) and Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), issued a statement in response to the Food and Drug Administration (FDA) announcement regarding the results of a safety review of Tumor Necrosis Factor (TNF) blockers [marketed as Remicade (infliximab), Enbrel (etanercept), Humira (adalimumab), Cimzia (certolizumab pegol) and Simponi (golimumab)]. This safety review was the subject of an FDA Early Communication in June 2008 pertaining to cases of malignancy in pediatric patients exposed to a TNF blocker. As a result of this review, the FDA has required strengthened warnings about the occurrence of lymphoma and other cancers in children and young adults using these medicines. AMGEN AND WYETH STATEMENT: Amgen and Wyeth believe that ENBREL continues to offer a favorable benefit-risk relationship for patients with the diseases for which it is indicated to treat, including moderate to severe Juvenile Idiopathic Arthritis (JIA). JIA can be a serious and potentially debilitating condition. Amgen will work with the FDA to update the U.S. Prescribing Information, and Medication Guide for ENBREL as described in the FDA communication which can be read at http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm175803.htm. In addition, Amgen and Wyeth will communicate the revised product labeling to both physicians and patients. ENBREL was first approved for JIA in the U.S. in 1999. It is estimated through postmarketing data that approximately 13,847 pediatric patients have been treated with ENBREL globally through February 2009, accounting for approximately 44,600 patient-years of exposure.
    [Show full text]
  • Mvx List.Pdf
    MVX_CODE manufacturer_name Notes status last updated date manufacturer_id AB Abbott Laboratories includes Ross Products Division, Solvay Inactive 16-Nov-17 1 ACA Acambis, Inc acquired by sanofi in sept 2008 Inactive 28-May-10 2 AD Adams Laboratories, Inc. Inactive 16-Nov-17 3 ALP Alpha Therapeutic Corporation Inactive 16-Nov-17 4 AR Armour part of CSL Inactive 28-May-10 5 AVB Aventis Behring L.L.C. part of CSL Inactive 28-May-10 6 AVI Aviron acquired by Medimmune Inactive 28-May-10 7 BA Baxter Healthcare Corporation-inactive Inactive 28-May-10 8 BAH Baxter Healthcare Corporation includes Hyland Immuno, Immuno International AG,and North American Vaccine, Inc./acquired somInactive 16-Nov-17 9 BAY Bayer Corporation Bayer Biologicals now owned by Talecris Inactive 28-May-10 10 BP Berna Products Inactive 28-May-10 11 BPC Berna Products Corporation includes Swiss Serum and Vaccine Institute Berne Inactive 16-Nov-17 12 BTP Biotest Pharmaceuticals Corporation New owner of NABI HB as of December 2007, Does NOT replace NABI Biopharmaceuticals in this codActive 28-May-10 13 MIP Emergent BioSolutions Formerly Emergent BioDefense Operations Lansing and Michigan Biologic Products Institute Active 16-Nov-17 14 CSL bioCSL bioCSL a part of Seqirus Inactive 26-Sep-16 15 CNJ Cangene Corporation Purchased by Emergent Biosolutions Inactive 29-Apr-14 16 CMP Celltech Medeva Pharmaceuticals Part of Novartis Inactive 28-May-10 17 CEN Centeon L.L.C. Inactive 28-May-10 18 CHI Chiron Corporation Part of Novartis Inactive 28-May-10 19 CON Connaught acquired by Merieux Inactive 28-May-10 21 DVC DynPort Vaccine Company, LLC Active 28-May-10 22 EVN Evans Medical Limited Part of Novartis Inactive 28-May-10 23 GEO GeoVax Labs, Inc.
    [Show full text]
  • FDA Listing of Authorized Generics As of July 1, 2021
    FDA Listing of Authorized Generics as of July 1, 2021 Note: This list of authorized generic drugs (AGs) was created from a manual review of FDA’s database of annual reports submitted to the FDA since January 1, 1999 by sponsors of new drug applications (NDAs). Because the annual reports seldom indicate the date an AG initially entered the market, the column headed “Date Authorized Generic Entered Market” reflects the period covered by the annual report in which the AG was first reported. Subsequent marketing dates by the same firm or other firms are not included in this listing. As noted, in many cases FDA does not have information on whether the AG is still marketed and, if not still marketed, the date marketing ceased. Although attempts have been made to ensure that this list is as accurate as possible, given the volume of d ata reviewed and the possibility of database limitations or errors, users of this list are cautioned to independently verify the information on the list. We welcome comments on and suggested changes (e.g., additions and deletions) to the list, but the list may include only information that is included in an annual report. Please send suggested changes to the list, along with any supporting documentation to: [email protected] A B C D E F G H I J K L M N O P Q R S T U V X Y Z NDA Applicant Date Authorized Generic Proprietary Name Dosage Form Strength Name Entered the Market 1 ACANYA Gel 1.2% / 2.5% Bausch Health 07/2018 Americas, Inc.
    [Show full text]
  • 1 2 3 4 5 6 7 8 ABCDEFG First Name Last Name
    ABC D E F G Consultant, Speakers Bureau Stock or Other Financial 1 First Name Last Name Institution Grant/Research Support or Advisory Board Member Options University of Texas Southwestern Medical 2 Kenneth Altshuler MD Center Dallas Janssen Abbott, Bristol‐Myers Squibb, Eli Lilly, Forest, Janssen, AstraZeneca, Bristol‐ AstraZeneca, Pfizer, Myers Squibb. Eli Lilly, 3 Lori Altshuler MD UCLA Abbott GlaxoSmithKline, Wyeth GlaxoSmithKline Western Psychiatric Institute Shire, Schering‐Plough, Jazz, 4 Boris Birmaher MD Pittsburg, PA Forest Solvay Abbott, Bristol‐Myers Squibb, Elan, GlaxoSmithKline, Janssen, Johnson & Johnson, Abbott, GlaxoSmithKline, Lilly Research, Parke‐Davis, Janssen, Eli Lilly, Lilly Research, Abbott, AstraZeneca, Eli University of Texas Health Robert Wood Johnson and Sanofi‐Synthelabo, UCB Lilly, GlaxoSmithKline, 5 Charles Bowden MD Science Center San Antonio Smith Kline Beecham Pharma, AstraZeneca, Pfizer Janssen AstraZeneca, GlaxoSmithKline, Merck, Organon, Pfizer, Roche, 6 Robert Buchanan MD University of Maryland Janssen, Ortho‐McNeil Solvay, Wyeth Abbott, AstraZeneca, Bristol‐ Myers Squibb, Eli Lilly, Abbott, AstraZeneca, Bristol‐ Abbott, AZ, BMS, Eli Lilly, Janssen, Pfizer, Solvay, Myers Squibb, Eli Lilly, Janssen, Janssen, Pfizer, Alamo, 7 Peter Buckley MD Medical College of Georgia Novartis Merck, Pfizer, Alamo, Novartis AstraZeneca Abbott, AstraZeneca, Merck, Abbott, AstraZeneca, Bristol‐ GlaxoSmithKline, Janssen, Eli Myers Squibb/Otsuka, Eli Lilly, Lilly, Pfizer, Ciba‐Geigy, GlaxoSmithKline, Janssen, Robert Wood
    [Show full text]
  • Amgen and Wyeth Statement on Outcome of Dermatologic and Ophthalmic Drugs Advisory Committee (DODAC) Meeting
    Amgen and Wyeth Statement on Outcome of Dermatologic and Ophthalmic Drugs Advisory Committee (DODAC) Meeting June 18, 2008 FDA Advisory Committee Recommends Enbrel(R) (etanercept) for the Treatment of Children and Adolescents with Chronic Moderate to Severe Plaque Psoriasis THOUSAND OAKS, Calif. & COLLEGEVILLE, Pa.--(BUSINESS WIRE)--June 18, 2008--Amgen (NASDAQ: AMGN) and Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), today issued the following statement on the outcome of today's meeting of the U.S. Food and Drug Administration's (FDA) Dermatologic and Ophthalmologic Drug Advisory Committee (DODAC) regarding the expanded use of ENBREL in treating pediatric patients with chronic moderate to severe plaque psoriasis. AMGEN AND WYETH STATEMENT: The Committee recommended, with an 8-5 vote, to approve ENBREL for the treatment of moderate to severe plaque psoriasis in children. The DODAC panel also provided input to the FDA regarding use in patients with more severe plaque psoriasis. Amgen and Wyeth are pleased the Committee adopted a position that is consistent with both companies' perspective that the benefits outweigh the risks in the population studied and that use should be reserved for appropriate patients. Amgen and Wyeth are hopeful that today represents an important step forward in working with the FDA to provide new treatment options for children living with moderate to severe plaque psoriasis. Despite the major impact this disease has on the lives of children and adolescents, there are currently no topical or systemic options approved in the U.S. for chronic use in this population. An expanded indication for ENBREL would address the unmet medical need for an approved and well-studied therapy in this small, under-served pediatric psoriasis patient population.
    [Show full text]
  • The Pfizer-Wyeth and Merck-Schering Plough Mergers
    <:. t>-'- iRAOE COM!I.1/S ~\)'C-"0RECEIVED DOCUMENTS S~ . NOV 1 3111119 ) '­ ./' Comments Submitted to the Federal Trade Commission o~/" the Pfizer-Wyeth and Merck-Schering Plough Mergers William S. Comanor and F. M. Scherer University ofCalifornia Harvard University Santa Barbara and Los Angeles Introduction We are both former Directors ofthe Bureau ofEconomics at the Federal Trade Commission, and have studied, lectured and written on the economics ofthe pharmaceutical industry for many years. As such, we feel obliged to submit these comments to the Commission because, in our judgment, both the Pfizer-Wyeth and Merck-Schering Plough mergers will further retard the rate ofpharmaceutical innovation and impose substantial consumer harm. This is an important matter, and we urge the Federal Trade Commission to consider these issues more fully. Pharmaceutical innovation is critically important for continued improvements in public health. l And for many decades, the major pharmaceutical companies have played an essential role in sustaining a rapid pace ofpharmaceutical innovation. Society has benefited greatly from their efforts. In recent years, however, the productivity ofthe innovation process has declined. The leading companies have spent increasing amounts on research and development without showing a corresponding increase in the number ofnew products introduced. Some companies have responded by seeking refuge in the greater scale achieved I H.E. Frech and Richard D. Miller, Health Care Matters: Pharmaceuticals, Obesity and the Quality ofLife, American Enterprise Institute, 2004. 1 through mergers. For the reasons outlined below, we believe that such efforts will merely depress further the rate ofinnovation. Many ofour views on these matters are contained in two earlier statements posted on the web site ofthe American Antitrust Institute, with whom we are both affiliated.
    [Show full text]
  • In the United States District Court for the District Of
    IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF DELAWARE PFIZER INC;, et al., ) ) Plaintiffs, ) ) v. ) Civ. No. 15-960-SLR ) MYLAN INC., et al., ) ) Defendants. ) ) Jack B. Blumenfeld, Esquire and Maryellen Noreika, Esquire of Morris Nichols, Arsht & Tunnell LLP, Wilmington, Delaware. Counsel for Plaintiffs. David E. Moore, Esquire, Bindu A. Palapura, Esquire, and Stephanie E. O'Byrne, Esquire of Potter Anderson & Corroon LLP, Wilmington, Delaware. Counsel for Defendants. Of Counsel: Robert L. Florence, Esquire, Karen L. Carroll, Esquire, and Micheal L. Binns, Esquire, Melanie Black Dubis, Esquire of Parker, Poe, Adams & Bernstein LLP. MEMORANDUM OPINION Dated: August \} , 2016 Wilmington, Delaware ROBINSON~ I. INTRODUCTION On October 22, 2015, Pfizer Inc., Wyeth LLC, Pfizer Pharmaceuticals LLC, PF PRISM C.V., ~nd Pfizer Manufacturing Holdings LLC, (collectively "plaintiffs") filed a complaint alleging infringement of three patents related to its injectable antibiotic product TYGACIL ® ("Tygacil") against defendants Mylan Inc., Mylan N.V., Mylan Laboratories Ltd. ("MLL"), and Mylan Pharmaceuticals ("MPI") (collectively "defendants"). (D.I. 1) Presently before the court is defendants' motion to dismiss for lack of personal jurisdiction and improper venue. (D.I. 6) Defendants Mylan Inc., Mylan N.V., and MPI have also filed a motion dismiss for failure to state a claim. (Id.) The court has jurisdiction over this matter pursuant to 28 U.S.C. §§ 1331 and 1338(a). II. BACKGROUND A. The parties Plaintiff Pfizer Inc. is a corporation organized and existing under the laws of the State of Delaware with a principal place of business in New York, New York. (D.I. 1 at~ 2) Plaintiff Wyeth LLC is a Delaware limited liability company with a principal place of business in New York, New York.
    [Show full text]
  • Rebateable Manufacturers
    Rebateable Labelers – July 2021 Manufacturers are responsible for updating their eligible drugs and pricing with CMS. Montana Healthcare Programs will not pay for an NDC not updated with CMS. Note: Some manufacturers on this list may have some NDCs that are covered and others that are not. Manufacturer ID Manufacturer Name 00002 ELI LILLY AND COMPANY 00003 E.R. SQUIBB & SONS, LLC. 00004 HOFFMANN-LA ROCHE 00006 MERCK & CO., INC. 00007 GLAXOSMITHKLINE 00008 WYETH PHARMACEUTICALS LLC, 00009 PHARMACIA AND UPJOHN COMPANY LLC 00013 PFIZER LABORATORIES DIV PFIZER INC 00015 MEAD JOHNSON AND COMPANY 00023 ALLERGAN INC 00024 SANOFI-AVENTIS, US LLC 00025 PFIZER LABORATORIES DIV PFIZER INC 00026 BAYER HEALTHCARE LLC 00032 ABBVIE INC. 00037 MEDA PHARMACEUTICALS, INC. 00039 SANOFI-AVENTIS, US LLC 00046 WYETH PHARMACEUTICALS INC. 00049 ROERIG 00051 ABBVIE INC 00052 ORGANON USA INC. 00053 CSL BEHRING L.L.C. 00054 HIKMA PHARMACEUTICAL USA, INC. 00056 BRISTOL-MYERS SQUIBB PHARMA CO. 00065 ALCON LABORATORIES, INC. 00068 AVENTIS PHARMACEUTICALS 00069 PFIZER LABORATORIES DIV PFIZER INC 00071 PARKE-DAVIS DIV OF PFIZER 00074 ABBVIE INC 00075 AVENTIS PHARMACEUTICALS, INC. 00078 NOVARTIS 00085 SCHERING CORPORATION 00087 BRISTOL-MYERS SQUIBB COMPANY 00088 AVENTIS PHARMACEUTICALS 00093 TEVA PHARMACEUTICALS USA, INC. 00095 BAUSCH HEALTH US, LLC Page 1 of 19 Manufacturer ID Manufacturer Name 00096 PERSON & COVEY, INC. 00113 L. PERRIGO COMPANY 00115 IMPAX GENERICS 00116 XTTRIUM LABORATORIES, INC. 00121 PHARMACEUTICAL ASSOCIATES, INC. 00131 UCB, INC. 00132 C B FLEET COMPANY INC 00143 HIKMA PHARMACEUTICAL USA, INC. 00145 STIEFEL LABORATORIES, INC, 00168 E FOUGERA AND CO. 00169 NOVO NORDISK, INC. 00172 TEVA PHARMACEUTICALS USA, INC 00173 GLAXOSMITHKLINE 00178 MISSION PHARMACAL COMPANY 00185 EON LABS, INC.
    [Show full text]
  • 20 Initiative: Pursuing a Global Commitment to Develop 10 New Antibacterial Drugs by 2020
    IDSA PUBLIC POLICY The 10 ϫ ‘20 Initiative: Pursuing a Global Commitment to Develop 10 New Antibacterial Drugs by 2020 Infectious Diseases Society of Americaa Infectious Diseases Society of America, Arlington, Virginia The time has come for a global commitment to develop new antibacterial drugs. Current data document the impending disaster due to the confluence of decreasing investment in antibacterial drug research and devel- opment concomitant with the documented rapid increase in the level of resistance to currently licensed drugs. Despite the good faith efforts of many individuals, professional societies, and governmental agencies, the looming crisis has only worsened over the past decade. THE PROBLEM fectively “escape” the effects of approved antibacterial drugs [1, 3]. Drug-resistant infections and related morbidity and The antibiotic pipeline problem may change the mortality are on the rise in the United States and practice of medicine as we know it. Advanced inter- around the world. The World Health Organization has ventions currently taken for granted—for example, sur- identified antimicrobial resistance as 1 of the 3 greatest gery, cancer treatment, transplantation, and care of pre- threats to human health. Two recent reports—one by mature babies—could become impossible as antibiotic the Infectious Diseases Society of America (IDSA) [1] options become fewer. Resistance to the current library and another by the European Centre for Disease Pre- of antibacterial drugs is a serious problem in all parts vention and Control and the European Medicines of the world including the Asia-Pacific region, Latin Agency [2]—demonstrate that there are few candidate America, Europe, and North America.
    [Show full text]