FDA NDC Directory · JSON-LD · Markdown

PANTOPRAZOLE SODIUM

NDC 51655-744 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic namePANTOPRAZOLE
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202882
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (20 mg/1)
Marketing started20210709
Package count1

External sources

Source: openFDA. Public-domain (CC0).