FDA NDC Directory · JSON-LD · Markdown

Omeprazole

NDC 65841-759 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA091352
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (10 mg/1)
Marketing started20121123
Package count5

External sources

Source: openFDA. Public-domain (CC0).