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Articles: Drug/Product Alerts |
Prior Articles
KINAXO's Cellular Target Profiling reveals mTOR as a new target of Celebrex
b3c newswire, 07/07/09
Shire has filed a treatment protocol for velaglucerase alfa for Gaucher Disease
Shire, 07/07/09 Tadalafil (Adcirca): Phosphodiesterase type 5 inhibitor approved for the treatment of pulmonary arterial hypertension (WHO Group I)
Formulary, 07/06/09 Teva Announces Approval and Launch of Tri-Lo Sprintec Tablets
Teva Pharmaceutical Industries, 07/02/09
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Teva and Antares Announce FDA Approval of Needle-Free Injector Product for Administration of Tev-Tropin (Human Growth Hormone)
Teva Pharmaceutical Industries, 07/01/09
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Cephalon Submits NUVIGIL Supplemental New Drug Application for the Treatment of Excessive Sleepiness Associated with Jet Lag Disorder
Cephalon, 07/01/09
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FDA Grants LUCAS 2 Chest Compression System 510(k) Clearance in the United States
Medtronic, 06/30/09
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European Approval for UCB's Cimzia
PharmExec, 06/29/09 Approval of Partial Change of API Manufacturing Method and Pharmaceutical Formulation of the Recombinant Human Erythropoietin "Epogin Injection"
Chugai Pharmaceutical Co., 06/29/09
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Once-yearly Aclasta approved in EU to treat osteoporosis caused by steroid treatment in men and postmenopausal women
Novartis, 06/29/09
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Sandoz receives approval for first-ever Japanese biosimilar
Novartis, 06/26/09
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Maine legislature approves pharmacist immunization
American Pharmacists Association, 06/25/09
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Watson Pharmaceuticals Receives FDA Approval For Generic PLAN B(R)
Watson Pharmaceuticals, 06/25/09
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Abbott Receives CE Mark for Company's Next-Generation XIENCE PRIME Drug Eluting Stent, Advancing Leadership Position
Abbott, 06/24/09 New Avatec Plus 3-Nitro Combination-Use Approval Now Brings Turkey Growers the Only Ionophore-Based Coccidiosis Control with the Performance of 3-Nitro
King Pharmaceuticals, 06/24/09
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Medtronic Receives CE Mark for Second-Generation MRI Pacemaker
Medtronic, 06/22/09
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New biological therapy Ilaris approved in US to treat children and adults with CAPS, a serious life-long auto-inflammatory disease
Novartis, 06/19/09
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BioMimetic Therapeutics Submits First Two PMA Modules to FDA; Company Receives ISO 9001 Certification and ISO 13485 Recertification
BioMimetic Therapeutics, 06/18/09 Mylan Receives FDA Approval for Additional Strength of Generic Restoril
Mylan, 06/18/09 Approval of Partial Change of API Manufacturing Method and Pharmaceutical Formulation of the Recombinant Human Erythropoietin "Epogin Injection"
Chugai Pharmaceutical Co., 06/17/09
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Indexed Journals: Expert Opinion in Pharmacotherapy, Formulary, U.S.Pharmacist
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142 Available Pages
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