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Pantoprazole sodium

NDC 71839-122 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerBE Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216171
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/10mL)
Marketing started20220525
Package count3

External sources

Source: openFDA. Public-domain (CC0).