FDA NDC Directory · JSON-LD · Markdown

PANTOPRAZOLE SODIUM

NDC 72603-317 · HUMAN PRESCRIPTION DRUG · GRANULE, DELAYED RELEASE

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213725
Dosage form / routeGRANULE, DELAYED RELEASE · ORAL
Active ingredientsPANTOPRAZOLE SODIUM (40 mg/1)
Marketing started20241001
Package count1

External sources

Source: openFDA. Public-domain (CC0).