FDA NDC Directory · JSON-LD · Markdown

Acid Reducer

NDC 58602-729 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Generic nameOmeprazole
Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206877
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE MAGNESIUM (20 mg/1)
Marketing started20180606
Package count7

External sources

Source: openFDA. Public-domain (CC0).