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Omeprazole

NDC 0781-2785 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA075757
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (10 mg/1)
Marketing started20030128
Package count3

External sources

Source: openFDA. Public-domain (CC0).