FDA approves first generic version of epilepsy drug Sabril from Teva

17 January 2019
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The US Food and Drug Administration (FDA) approved the first generic version of Sabril (vigabatrin) Tablets manufactured by Teva Pharmaceutical Industries (NYSE: TEVA) US subsidiary, for treating complex partial seizures, as an adjunctive therapy (given with another primary treatment) in patients 10 years and older who have responded inadequately to several alternative (refractory) treatments.

This approval helps to provide a safe, effective, quality, and affordable treatment option for certain patients, the agency stated.

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