FDA NDC Directory · JSON-LD · Markdown

Omeprazole

NDC 68462-397 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA091672
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (40 mg/1)
Marketing started20141031
Package count4

External sources

Source: openFDA. Public-domain (CC0).