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RABEPRAZOLE SODIUM

NDC 72888-059 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic namerabeprazole sodium
Labeler / ManufacturerAdvagen Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204237
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsRABEPRAZOLE SODIUM (20 mg/1)
Marketing started20170601
Package count2

External sources

Source: openFDA. Public-domain (CC0).