FDA NDC Directory · JSON-LD · Markdown

Pantoprazole

NDC 80425-0552 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077619
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (20 mg/1)
Marketing started20251015
Package count3

External sources

Source: openFDA. Public-domain (CC0).