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Zydus Lifesciences-led arm bags US FDA approval for Brivaracetam tabs

Zydus Lifesciences-led arm bags US FDA approval for Brivaracetam tabs

The United States Food and Drug Administration (USFDA) has granted final permission to Zydus Lifesciences' (previously Cadila Healthcare Limited) U.S. subsidiary Zydus Pharmaceuticals (USA) to commercialise Brivaracetam Tablets USP 10 mg, 25 mg, 50 mg, 75 mg, and 100 mg.

Zydus was one of the first ANDA applicants to submit a substantially complete ANDA for Brivaracetam Tablets USP 10 mg, 25 mg, 50 mg, 75 mg, and 100 mg with a paragraph IV certification. Brivaracetam tablets are therefore eligible for 180 days of shared generic medication exclusivity. Brivaracetam is approved for the treatment of partial-onset seizures in children aged 4 and above.

The medicine would be produced at the group's formulation manufacturing plant in Ahmedabad Special Economic Zone.

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USFDA Zydus Lifesciences
More news about: quality / gmp | Published by Sudeep Soparkar | October - 06 - 2022 | 206

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