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Articles: Drug/Product Approvals |
Prior Articles
Acura Pharmaceuticals and King Pharmaceuticals Provide Update on ACUROX® NDA
King Pharmaceuticals, 09/04/09
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Shire Announces FDA Approval of Once-Daily INTUNIV? (guanfacine) Extended Release Tablets for the Treatment of ADHD in Children and Adolescents Aged 6 to 17
Shire, 09/04/09 FDA Approves Valcyte (valganciclovir hydrochloride) to Prevent Cytomegalovirus (CMV) Disease in Pediatric Patients Who Receive Heart or Kidney Transplants
Roche, 09/02/09
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Update on FDA Registration of Actemra, a Humanized Anti-Human IL-6 Receptor Monoclonal Antibody for Rheumatoid Arthritis
Chugai Pharmaceutical Co., 09/02/09
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FDA Approves New Imaging Modules
HealthDataManagement, 09/01/09 Insecticide Movento granted regulatory approval in Australia
BayNews International, 09/01/09
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AstraZeneca announces FDA acceptance of New Drug Application for VIMOVO
AstraZeneca, 09/01/09
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Watson Pharmaceuticals Receives FDA Approval for Generic PLAN B for Over-the-Counter Use
Watson Pharmaceuticals, 08/31/09
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Panel Will Consider Clinical Data Supporting Approval and Labeling
Genzyme, 08/31/09
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Update on FDA Registration of Actemra, a Humanized Anti-Human IL-6 Receptor Monoclonal Antibody for Rheumatoid Arthritis
Chugai Pharmaceutical Co., 08/31/09
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Medtronic Board Approves Second Quarter Cash Dividend for Fiscal Year 2010
Medtronic, 08/28/09
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APP Pharmaceuticals Receives Approval for Penicillin G Potassium for Injection, USP
American Pharmaceutical Partners, 08/26/09
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Health Canada Approves Abbott's XIENCE V Drug Eluting Stent
Abbott, 08/25/09 Novartis receives approval in EU for Xolair to treat children age 6 to 11 years suffering from severe persistent allergic asthma
Novartis, 08/25/09
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Salix Pharmaceuticals Announces FDA Acceptance for Filing and Priority Review Designation for Rifaximin NDA for the Maintenance of Remission of Hepatic Encephalopathy
Salix Pharmaceuticals, 08/25/09
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Update on FDA Registration of Actemra, a Humanized Anti-Human IL-6 Receptor Monoclonal Antibody for Rheumatoid Arthritis
Chugai Pharmaceutical Co., 08/24/09
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Warner Chilcott Completes Irish Redomestication
Warner Chilcott, 08/24/09 Merck is Pleased the FDA and CDC Re-affirm the Safety Profile of GARDASIL [Human Papillomavirus Quadrivalent (Types 6, 11, 16 and 18) Vaccine, Recombinant]
Merck & Co., 08/21/09
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Bristol-Myers Squibb Announces Preliminary Court Approval of Derivative Settlement
Bristol Myers-Squibb Company, 08/21/09
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Dey Issues Advisory
Mylan, 08/21/09
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Indexed Journals: U.S.Pharmacist, FDA Drug Alerts, Pharmiweb
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