Aurobindo Pharma Gets US FDA Approval for Perampanel Tablets

MT Newswires Live
Oct 05

Aurobindo Pharma (NSE:AUROPHARMA, BOM:524804) received final approval from the U.S. Food and Drug Administration to manufacture and market Perampanel Tablets in strengths ranging from 2 mg to 12 mg, according to an Oct. 3 exchange filing.

The product will be manufactured at Unit-IV of APL Healthcare, a wholly owned subsidiary, and launched in the third quarter of fiscal 2027.

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