FDA NDC Directory · JSON-LD · Markdown

omeprazole

NDC 56062-401 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Generic nameOmeprazole
Labeler / ManufacturerPublix Super Markets Inc
Marketing categoryNew Drug Application (innovator) · App NDA022032
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20220701
Package count2

External sources

Source: openFDA. Public-domain (CC0).