USFDA gives approval for Ranolazine ER tablets

Ranolazine Extended-Release Tablets, 500 mg, and 1000 mg are indicated for the treatment of chronic angina.

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USFDA Approval
USFDA Approval

Last Updated on October 15, 2024 by The Health Master

Unichem Laboratories has received ANDA approval for its ranolazine extended-release tablets, 500 mg and 1000 mg from the United States Food and Drug Administration (USFDA).

This drug approval is to market a generic version of Ranexa (ranolazine extended-release tablets) 500 mg and 1000 mg, of Gilead Sciences.

Ranolazine Extended-Release Tablets, 500 mg, and 1000 mg are indicated for the treatment of chronic angina.

The product will be commercialised from Unichem’s Goa Plant.

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