USFDA gives tentative nod for Gabapentin Tablets, 300 mg and 600 mg

USFDA gives tentative nod to Zydus Lifesciences for Gabapentin Tablets, 300 mg and 600 mg

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USFDA Drug product Approval
USFDA Approval

Last Updated on December 31, 2023 by The Health Master

Zydus Lifesciences has received tentative approval from the United States Food and Drug Administration (USFDA) for Gabapentin Tablets (Once-Daily), 300 mg and 600 mg.

Gabapentin tablets are indicated for the management of Postherpetic Neuralgia (PHN).

The drug will be manufactured at the group’s formulation manufacturing facility at Moraiya.

Gabapentin Tablets had annual sales of $90 million in the United States (IQVIA MAT Dec. 2022).

The group now has 343 approvals and has so far filed over 440 ANDAs since the commencement of the filing process in FY 2003-04.

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