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Pantoprazole Sodium

NDC 68071-1963 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerNuCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090074
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20110120
Package count3

External sources

Source: openFDA. Public-domain (CC0).