FDA NDC Directory · JSON-LD · Markdown

Pantoprazole Sodium DR

NDC 72189-514 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA202882
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20230911
Package count2

External sources

Source: openFDA. Public-domain (CC0).