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Omeprazole

NDC 58602-837 · HUMAN OTC DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213201
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE MAGNESIUM (20 mg/1)
Marketing started20230428
Package count1

External sources

Source: openFDA. Public-domain (CC0).