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up and up omeprazole

NDC 11673-346 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Generic nameomeprazole
Labeler / ManufacturerTarget Corporation
Marketing categoryNew Drug Application (innovator) · App NDA022032
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20220203
Package count1

External sources

Source: openFDA. Public-domain (CC0).