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PANTOPRAZOLE SODIUM

NDC 59651-671 · HUMAN PRESCRIPTION DRUG · GRANULE, DELAYED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA217923
Dosage form / routeGRANULE, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20250331
Package count1

External sources

Source: openFDA. Public-domain (CC0).