FDA NDC Directory · JSON-LD · Markdown

RABEPRAZOLE SODIUM

NDC 72189-142 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA205761
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsRABEPRAZOLE SODIUM (20 mg/1)
Marketing started20201015
Package count2

External sources

Source: openFDA. Public-domain (CC0).