FDA NDC Directory · JSON-LD · Markdown

pantoprazole sodium

NDC 70010-191 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217282
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20240412
Package count2

External sources

Source: openFDA. Public-domain (CC0).