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Pantoprazole Sodium

NDC 55150-202 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerEugia US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205675
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20160330
Package count2

External sources

Source: openFDA. Public-domain (CC0).