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Pantoprazole Sodium

NDC 0904-6870 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA202038
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20120928
Package count1

External sources

Source: openFDA. Public-domain (CC0).