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PANTOPRAZOLE SODIUM

NDC 31722-712 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic namePANTOPRAZOLE
Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202882
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (20 mg/1)
Marketing started20140910
Package count3

External sources

Source: openFDA. Public-domain (CC0).