FDA NDC Directory · JSON-LD · Markdown

OMEPRAZOLE

NDC 59640-699 · HUMAN OTC DRUG · CAPSULE, DELAYED RELEASE

Generic nameOmeprazole
Labeler / ManufacturerH E B
Marketing categoryAbbreviated NDA (generic) · App ANDA216096
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20260807
Package count2

External sources

Source: openFDA. Public-domain (CC0).