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Lannett Company, Inc. (NYSE AMEX: LCI) announced that 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. According to Wolters Kluwer, U.S. sales of Phentermine Hydrochloride Capsules USP, 30 mg (more…)

WASHINGTON (AP) — A pink pi ll designed to boost sex drive in women — the latest attempt by the drug industry to find a female equivalent to Viagra — fell short in two studies, federal health regulators said Wednesday.

The Food and… (Source: OrlandoSentinel: Medical Research)

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Lannett Company, Inc. (Amex:LCI) announced it has received approval from the U.S. Food and Drug Administration (FDA) for the company’s supplemental Abbreviated New Drug Application (ANDA) of Phentermine Hydrochloride Capsules 30 mg. The company expects to commence marketing this product immediately. Phentermine Hydrochloride (HCl) is indicated for the short-term management of obesity. [cl ick link for full article] (Source: Obesity / Weight Loss (more…)

Source: BioS pace
Area: News
According to BioSpace, a New Drug Application (NDA) has been submitted to the US FDA seeking approval of Qnexa® (controlled-release oral formulation of low dose phentermine and topiramate) for the treatment of obesity, including weight loss and maintenance of weight loss, in patients who are obese or overweight with co-morbidities such as hypertension, type 2 diabetes, dyslipidaemia or central adiposity.  (more…)

DETROIT, Aug. 22 (HSMN NewsFeed) — Caraco Pharmaceutical Laboratories, Ltd., (Amex: CPD ) announce d today that the US Food and Drug Administration (FDA) has granted final approval for the Company’s Abbreviated New Drug Application (ANDA) for Phentermine… Biopharmaceuticals, Generics, FDACaraco Pharmaceutical, Phentermine, Adipex-P, TEVA Pharmaceutical (Source: HSMN NewsFeed)

Barr Laboratories, Inc., a subsidiary of Barr Pharmaceuticals, Inc. (NYSE: BRL), today announced that it received final approval from the U.S. Food and Drug Administration (FDA) for its application to manu facture and market ageneric version of Pfizer Inc.’s XANAX XR(R) (Alprazolam Extended-Release)Tablets, 0.5 mg, 1 mg, 2 mg and 3 mg. The Company intends to launch itsproduct immediately. [click link for full article] (Source: Psychology / Psychiatry (more…)

Barr Laboratories, Inc., a subsidiary of Barr Pharmaceuticals, Inc. (NYSE: BRL), today announced that it received final approval from the U.S. Food and Drug Administration (FDA) for its application to manufacture and market ageneric version of Pfizer Inc.’s XANAX XR(R) (Alprazolam Extended-Release)Tablets, 0.5 mg, 1 mg, 2 mg and 3 mg. The Company intends to launch itsproduct immediately. [click link for full article] (Source: Health N ews from (more…)

Global Pharmaceuticals Division to Launch

HAYWARD, Calif.–(HSMN NewsFeed)–IMPAX Laboratories, Inc. (OTC:IPXL ) today announced that the U.S. Food and Drug Administration (FDA) has granted final approval of the Company’s Abbreviated New Drug Applicatio… Biopharmaceuticals, Generics, FDAIMPAX Laboratories, Xanax, Alprazolam, Xanax XR, Pharmaci a (Source: HSMN NewsFeed)

Actavis Group, the international generic pharmaceuticals company, today announced that it has received approval from the U.S. Food & Drug Administration to market Alprazolam orally disintegrating tablets. Distribution of the product will commence immediately. (Source: Pharmaceutical Online News)

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Lannett Company, Inc. (Amex:LCI) announced it has received approval from the U.S. Food and Drug Administration (FDA) for the company’s supplemental Abbreviated New Drug Application (ANDA) of Phentermine Hydrochloride Capsules 30 mg. The company expects to commence marketing th is product immediately. Phentermine Hydrochloride (HCl) is indicated for the short-term management of obesity. [click link for full article] (Source: Obesity / Weight Loss (more…)