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Articles: Drug/Product Alerts |
Prior Articles
FDA Approves Boston Scientific's Next-Generation TAXUS Liberte Atom Stent System
Boston Scientific, 05/28/09
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Angiotech pharmaceuticals announces fda approval of nextgeneration taxus liberte atom stent
Angiotech Pharmaceuticals, 05/28/09
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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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European approvals for Levocetirizine
Synthon, 05/26/09
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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., 05/22/09
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Medtronic Announces FDA Approval of Two Deep Brain Stimulation Devices That Offer Programming Advances and New Tools for Patients with Movement Disorders
Medtronic, 05/22/09
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Taro Receives FDA Approval for Sulfacetamide Sodium Topical Suspension ANDA
Taro Pharmaceuticals USA, 05/22/09
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Avigen Granted AV411 Patent for Neuropathic Pain
Avigen, 05/21/09
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Nexavar Approved in Japan for the Treatment of Advanced Liver Cancer
BayNews International, 05/21/09
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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., 05/21/09
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Nexavar Approved in Japan for the Treatment of Advanced Liver Cancer
Onyx Pharmaceuticals, 05/21/09
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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., 05/20/09
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Genentech and Biogen Idec Submit Applications to the FDA for Rituxan for Most Common Type of Adult Leukemia
Genentech, 05/20/09
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Endeavor Drug-Eluting Stent Is First to Receive CE Mark for Treating Acute Coronary Syndrome
Medtronic, 05/20/09
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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., 05/19/09
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DA Grants Approval for Use of RISPERDAL CONSTA as Both a Monotherapy and Adjunctive Therapy in the Maintenance Treatment of Bipolar I Disorder
Janssen, 05/19/09
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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., 05/18/09
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Indexed Journals: Expert Opinion in Pharmacotherapy, Formulary, U.S.Pharmacist
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143 Available Pages
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