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Omeprazole

NDC 59726-744 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerP & L Development, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206582
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE MAGNESIUM (20 mg/1)
Marketing started20250829
Package count1

External sources

Source: openFDA. Public-domain (CC0).