FDA NDC Directory · JSON-LD · Markdown

Omeprazole

NDC 62175-114 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic nameomeprazole
Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075410
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (10 mg/1)
Marketing started20030903
Package count4

External sources

Source: openFDA. Public-domain (CC0).