Zydus Lifesciences Receives USFDA Tentative Nod for Generic Multiple Sclerosis Drug
Zydus Lifesciences has received tentative approval from the United States Food and Drug Administration (USFDA) for Diroximel Fumarate delayed-release capsules, 231 mg, a generic version of Vumerity delayed-release capsules of the same strength.
The United States Food And Drug Administration (US | 13/11/2025 | By Dineshwori | 108
Cipla's Bommasandra Facility Gets VAI Classification from USFDA
Cipla has announced that its manufacturing facility in Bommasandra, Bengaluru, has received a Voluntary Action Indicated (VAI) classification from the USFDA following a recent inspection.
The United States Food And Drug Administration (US | 06/08/2025 | By Dineshwori | 202
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