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Omeprazole

NDC 60505-3952 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerApotex Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA076048
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE (20 mg/1)
Marketing started20031111
Marketing ended20270131
Package count1

External sources

Source: openFDA. Public-domain (CC0).