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Pantoprazole sodium

NDC 70095-024 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerSun Pharmaceutical Industries Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204400
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/10mL)
Marketing started20230403
Package count2

External sources

Source: openFDA. Public-domain (CC0).