USFDA approves Sun Pharma's generic Flomax ANDA

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Jul 16 2010

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Sun Pharmaceutical Industries Ltd. (Reuters: SUN.BO, Bloomberg: SUNP IN, NSE:SUNPHARMA, BSE:524715) announced that USFDA has granted approval for its Abbreviated New Drug Application (ANDA) to market a generic version of Flomax ®, tamsulosin capsules.

These tamsulosin hydrochloride capsules, 0.4 mg are therapeutically equivalent to Flomax® Capsules 0.4 mg from Boehringer Ingelheim Pharmaceuticals, Inc.

Tamsulosin hydrochloride capsules are indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH).

SOURCE Sun Pharmaceutical Industries Ltd.

www.sunpharma.com

Posted in: Men's Health News | Pharmaceutical News

Tags: Benign Prostatic Hyperplasia, Cardiology, Gastroenterology, Hyperplasia, Neurology, New Drug Application, Pharmaceuticals, Psychiatry

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