News and FDA Updates for Lannett (NYSE:LCI), MannKind (NASDAQ:MNKD), Meridian (NASDAQ:VIVO)

M.E. Garza
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On 07/20/10, Lannett Company, Inc. (NYSE:LCI) announced it has received approval from the U.S. Food and Drug Administration (FDA) of its Abbreviated New Drug Application (ANDA) for Phentermine Hydrochloride Blue/White Seed Capsules USP, 30 mg, the generic equivalent of Sandoz, Inc.'s Reference Listed Drug (RLD) Phentermine Hydrochloride Capsules USP, 30 mg.

On 07/20/10, MannKind Corporation (NASDAQ:MNKD) announced it has submitted, and the U.S. Food and Drug Administration (FDA) has accepted, MannKind´s resubmission of its New Drug Application (NDA) for AFREZZA™ (insulin human [rDNA origin]) and classified it as a Class 2 resubmission.

On 07/20/10, Meridian Bioscience, Inc., (NASDAQ:VIVO) announces effective it will have completed the purchase of all the outstanding capital stock of he Bioline group of companies consisting of Bioline Ltd (UK), Bioline GmbH (Germany), Bioline (Aust) Pty Ltd (Australia), Bioline Reagents Ltd, and Bioline USA, Inc for $23.3 million in cash on hand.

Biotech investors interested in seeing more details about these stories and accessing the complete database of clinical trials and upcoming FDA decisions can access that information here:

http://biomedreports.com/fda-calendar/fda-calendar.html

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