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Omeprazole Magnesium

NDC 0363-0042 · HUMAN OTC DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerWalgreens Company
Marketing categoryAbbreviated NDA (generic) · App ANDA078878
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsOMEPRAZOLE MAGNESIUM (20 mg/1)
Marketing started20150901
Package count4

External sources

Source: openFDA. Public-domain (CC0).