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omeprazole

NDC 57483-840 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerINNOVUS PHARMACEUTICALS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA207891
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20200810
Package count1

External sources

Source: openFDA. Public-domain (CC0).