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Pantoprazole Sodium

NDC 65862-559 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202038
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (20 mg/1)
Marketing started20120928
Package count3

External sources

Source: openFDA. Public-domain (CC0).