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Pantoprazole Sodium

NDC 0143-9300 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryNew Drug Application (innovator) · App NDA209463
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20170922
Package count1

External sources

Source: openFDA. Public-domain (CC0).