USFDA gives final approval for Sodium Phenylbutyrate tablets

The statement said that the tablets will be distributed in the US by Glenmark Pharma Inc., USA.

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USFDA Approval
USFDA Approval

Last Updated on October 15, 2024 by The Health Master

The US Food and Drug Administration (USFDA) has given final approval to Glenmark Pharma’s sodium phenylbutyrate tablets USP, 500 mg.

This is the generic version of Buphenyl Tablets, 500 mg, of Horizon Therapeutics, according to a statement from Glenmark Pharma.

The statement said that the tablets will be distributed in the US by Glenmark Pharma Inc., USA.

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