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Omeprazole

NDC 71335-1395 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA076048
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (40 mg/1)
Marketing started20090121
Marketing ended20270131
Package count8

External sources

Source: openFDA. Public-domain (CC0).