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Pantoprazole Sodium

NDC 71288-600 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215860
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/10mL)
Marketing started20220829
Package count1

External sources

Source: openFDA. Public-domain (CC0).