FDA NDC Directory · JSON-LD · Markdown

omeprazole

NDC 72559-014 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerLittle Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207891
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20200715
Package count4

External sources

Source: openFDA. Public-domain (CC0).