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omeprazole

NDC 42507-414 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Generic nameOmeprazole
Labeler / ManufacturerHyVee Inc
Marketing categoryNew Drug Application (innovator) · App NDA022032
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20260128
Package count2

External sources

Source: openFDA. Public-domain (CC0).