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Rabeprazole Sodium

NDC 68788-7459 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208644
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsRABEPRAZOLE SODIUM (20 mg/1)
Marketing started20180427
Package count2

External sources

Source: openFDA. Public-domain (CC0).