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Pantoprazole

NDC 85509-1332 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerPHOENIX RX LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077619
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (20 mg/1)
Marketing started20110119
Package count3

External sources

Source: openFDA. Public-domain (CC0).