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Pantoprazole sodium delayed-release

NDC 70756-019 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLifestar Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215880
Dosage form / routeTABLET · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20220727
Package count2

External sources

Source: openFDA. Public-domain (CC0).