Watson’s patent issue

March 16, 2012

WATSON Laboratories is seeking US FDA approval to market nebivolol hydrochloride tablets, 2.5mg, 5mg, 10mg and 20mg, a generic version of Forest Laboratories' Bystolic (a beta-adrenergic blocking agent that is approved for the treatment of hypertension). Its application is being contested by Forest, who has filed a suit which seeks to stop Watson from commercialising its generic before the expiry of the drug’s patent. The commencement of the law suit has resulted in a stay of final FDA approval until 17 June 2015, or until final resolution of the matter before the court.

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Pharmacy Daily | Watson’s patent issue

Watson’s patent issue

Other recent headlines

RACGP slams SA move

PSA’s new vaping criteria

IPA makes room for charity

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES