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15 Mar 2012

Watson Laboratories Files ANDA for Generic Version of BYSTOLIC

Watson Laboratories has submitted an Abbreviated New Drug Application with the FDA to market Nebivolol Hydrochloride Tablets, a generic version of Forest Laboratories' BYSTOLIC.

Watson Pharmaceuticals, Inc. confirmed Wednesday that its subsidiary, Watson Laboratories, Inc., filed an Abbreviated New Drug Application (ANDA) with the U.S. FDA seeking approval to market Nebivolol Hydrochloride Tablets, 2.5 mg, 5 mg, 10 mg and 20 mg.

 

The ANDA product is a generic version of Forest Laboratories' BYSTOLIC, which is a beta-adrenergic blocking agent that is approved for the treatment of hypertension. For the twelve months ending January 31, 2012, BYSTOLIC had total U.S. sales of approximately $391 million according to IMS Health data.

 

Forest Laboratories filed suit against Watson on March 13, 2012, in the United States District Court for the District of Delaware seeking to prevent Watson from commercia

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