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Ferumoxytol

NDC 0781-3154 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameferumoxytol
Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA206604
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsFERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE (510 mg/17mL)
Marketing started20210715
Package count2

External sources

Source: openFDA. Public-domain (CC0).