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Esomeprazole Magnesium

NDC 58602-840 · HUMAN OTC DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214473
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsESOMEPRAZOLE MAGNESIUM DIHYDRATE (20 mg/1)
Marketing started20230712
Package count3

External sources

Source: openFDA. Public-domain (CC0).