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Protonix Delayed-Release

NDC 0008-0841 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic namePANTOPRAZOLE SODIUM
Labeler / ManufacturerWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Marketing categoryNew Drug Application (innovator) · App NDA020987
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20000501
Package count1

External sources

Source: openFDA. Public-domain (CC0).