FDA NDC Directory · JSON-LD · Markdown

Omeprazole

NDC 60687-608 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078490
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (40 mg/1)
Marketing started20210804
Package count1

External sources

Source: openFDA. Public-domain (CC0).