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Response Submitted To FDA Approvable Letter For Hypertension Compound Nebivolol
Forest Laboratories, announced that its licensing partner Mylan Laboratories submitted a response to the approvable letter issued by the United States...

Allergy Spray Veramyst Approved by FDA
The U.S. Food and Drug Administration approved once-daily Veramyst (fluticasone furoate) Nasal Spray to treat seasonal and year-round allergy symptoms...

Alma Lasers Receives FDA Clearance For The Accent Dual Mode RF System
lma Lasers, a global leader in laser, light-based and radio frequency (RF) technologies used in aesthetic medicine, announced today that it has receiv...

FDA Approves Lantus SoloStar A New Prefilled Disposable Insulin Pen For Use With LANTUS In People With Type 1 And Type 2 Diabetes
Sanofi-aventis announced that the U.S. Food and Drug Administration (FDA) approved Lantus SoloStar(R), a new prefilled disposable insulin pen for once...

InSite Vision Announces FDA Approval for AzaSite Approval Triggers $19 Million Milestone Payment
InSite Vision - an ophthalmic therapeutics, diagnostics and drug delivery company, announced that the U.S. Food & Drug Administration (FDA) has appr...

Inspire Announces FDA Approval Of AzaSite
Inspire Pharmaceuticals, said that the U.S. Food and Drug Administration (FDA) has approved AzaSite (azithromycin ophthalmic solution) 1% for the trea...

NIDEK Gains FDA Clearance for ORION, a New Auto-Retinal Imaging Device
NIDEK, speacialist in laser and diagnostic instrumentation for the optical and eye care industry, announced today that the U. S. Food & Drug Administr...

Arthrocare Receives FDA Clearance To Market Magnum PI Knotless Implant System
ArthroCare said that it has received 510 clearance from the U.S. Food and Drug Administration to market its Magnum PI Knotless Implant System, which u...

FDA and USDA Determine Swine Fed Adulterated Product
The USDA Food Safety and Inspection Service (FSIS) and the U.S. Food and Drug Administration (FDA) today notified State authorities that swine fed adu...

FDA Approves INVEGA For Long-Term Maintenance Treatment Of Schizophrenia
The U.S. Food and Drug Administration (FDA) today approved INVEGA (paliperidone) Extended-Release Tablets, a new once-daily, atypical antipsychotic, f...

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