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Omeprazole

NDC 0363-1607 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerWalgreens Company
Marketing categoryAbbreviated NDA (generic) · App ANDA207740
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20200115
Package count3

External sources

Source: openFDA. Public-domain (CC0).