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Pantoprazole Sodium

NDC 42799-952 · HUMAN PRESCRIPTION DRUG · GRANULE, DELAYED RELEASE

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA216247
Dosage form / routeGRANULE, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20230616
Package count1

External sources

Source: openFDA. Public-domain (CC0).