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Esomeprazole Magnesium

NDC 57483-225 · HUMAN OTC DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerINNOVUS PHARMACEUTICALS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA209339
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsESOMEPRAZOLE MAGNESIUM DIHYDRATE (20 mg/1)
Marketing started20230525
Package count1

External sources

Source: openFDA. Public-domain (CC0).