FDA NDC Directory · JSON-LD · Markdown

Rabeprazole Sodium

NDC 70518-2590 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA208644
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsRABEPRAZOLE SODIUM (20 mg/1)
Marketing started20200218
Package count1

External sources

Source: openFDA. Public-domain (CC0).