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Pantoprazole sodium

NDC 27241-256 · HUMAN PRESCRIPTION DRUG · FOR SUSPENSION

Labeler / ManufacturerAjanta Pharma USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217416
Dosage form / routeFOR SUSPENSION · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20230209
Package count2

External sources

Source: openFDA. Public-domain (CC0).