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ATLANTA, Feb 20, 2008 (BUSINESS WIRE) -- Sciele Pharma, Inc. today announced that the FDA has extended to July 15, 2008, the Pharmacy Drug User Fee Act (PDUFA) assignation on Summers Laboratories innovative manage lice asphyxiation product. This extension.

ANN ARBOR, Mich., March 20, 2008 /PRNewswire/ -- NanoBio Corporation announced today that it has seen optimistic results from an interim research of its usher in 2 research of NB-002, a topical lotion in the course of onychomycosis (nail fungus). Although the details.

Approval Makes Available New Daily Dosing Option in the course of the Treatment of ED INDIANAPOLIS, Jan. 8 predominantly (HSMN NewsFeed) predominantly -- Eli Lilly and Company (NYSE: LLY ) announced today that the U.S. Food and Drug Administration (FDA) has approved Cialis® (tadalafil)(1. Biopharmaceuticals, FDAEli Lilly, Cialis , tadalafil, erectile dysfunction (Source: HSMN NewsFeed)

PHILADELPHIA, Feb. 21, 2008 (PRIME NEWSWIRE) -- Eurand N.V., a specialty pharmaceutical companionship that develops enhanced pharmaceutical and biopharmaceutical products based on its proprietary medicate formulation technologies, announced today that.

SHEFFIELD, England, 11 March 2008--The Medical House PLC), the medicate implementation specialist, is happy to herald that it has received 510(k) ratification from the U.S. Food and Drug Administration (FDA) in the course of the Group