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Articles: Drug/Product Approvals |
Prior Articles
Approval of Partial Change of API Manufacturing Method and Pharmaceutical Formulation of the Recombinant Human Erythropoietin "Epogin Injection"
Chugai Pharmaceutical Co., 06/05/09
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Approval of Partial Change of API Manufacturing Method and Pharmaceutical Formulation of the Recombinant Human Erythropoietin "Epogin Injection"
Chugai Pharmaceutical Co., 06/04/09
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FDA advisory panel makes favorable recommendation for ARZERRA (ofatumumab)
GlaxoSmithKline, 06/02/09
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FDA approves Reclast to prevent osteoporosis in postmenopausal women with convenient less frequent dosing
Novartis, 06/02/09
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Approval of Partial Change of API Manufacturing Method and Pharmaceutical Formulation of the Recombinant Human Erythropoietin "Epogin Injection"
Chugai Pharmaceutical Co., 06/01/09
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Genzyme Receives Positive Opinion for European Approval of Mozobil
Genzyme, 06/01/09
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Afinitor recommended for use in the European Union for patients with advanced kidney cancer
Novartis, 06/01/09
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Fda advisory panel makes favorable recommendation for glaxosmithkline and genmab's arzerra (ofatumumab)
Genmab, 06/01/09
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Mylan Receives Tentative FDA Approval for Generic Version of Singulair
Mylan, 06/01/09 FDA Approves New Total Ankle Replacement System
FDA Press Releases, 05/29/09
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FDA Approves Besivance to Treat Bacterial Conjunctivitis
FDA Press Releases, 05/29/09
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Astellas receives fda approval for use of progra(tacrolimus)
in conjunction with mycophenolate mofetil (mmf) in kidney transplant recipients
Astellas, 05/29/09
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FDA Clears Boston Scientifics SpyScope Access and Delivery Catheter for Use in Endoscopic Procedures Throughout Pancreatico-Biliary System
Boston Scientific, 05/29/09
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Bevacizumab now approved for recurrent glioblastoma
American Pharmacists Association, 05/29/09
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Angiotech pharmaceuticals announces fda approval of nextgeneration taxus liberte atom stent
Angiotech Pharmaceuticals, 05/28/09
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FDA Approves Boston Scientific's Next-Generation TAXUS Liberte Atom Stent System
Boston Scientific, 05/28/09
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Allos Therapeutics Announces FDA Accepts Pralatrexate NDA for Filing and Grants the Application Priority Review Status
Allos Therapeutics, 05/27/09
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FDA Grants Full Approval for SPRYCEL (dasatinib) for the Treatment of Adults with Chronic Myeloid Leukemia Who Are Resistant or Intolerant to Prior Therapies Including Gleevec
Bristol Myers-Squibb Company, 05/27/09
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FDA Approves Samsca to Treat Hyponatremia
FDA Press Releases, 05/26/09
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U.S. Department of Agriculture grants approval for Bayer CropScience's GlyTol cotton technology
BayNews International, 05/26/09
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