Zydus receives FDA’s tentative approval for Budesonide delayedrelease capsules, 4 mg
Drug Approval

Zydus receives FDA’s tentative approval for Budesonide delayedrelease capsules, 4 mg

Budesonide is indicated for mild to moderate active Crohn's disease involving the ileum and/or the ascending colon in adults and children 8 years of age and olde

  • By IPP Bureau | November 05, 2025

Zydus Lifesciences Limited has received tentative approval from the United States Food and Drug Administration (USFDA) for Budesonide delayed-release capsules, 4 mg (USRLD: Tarpeyo Capsules, 4 mg).

Budesonide is indicated for mild to moderate active Crohn's disease involving the ileum and/or the ascending colon in adults and children 8 years of age and older. Budesonide capsules will be produced at is Zydus Pharmaceuticals Ltd, SEZ-II.

The group now has 425 approvals and has so far filed 487 ANDAs since the commencement of the filing process in FY 2003-04.

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