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Gadoterate Meglumine

NDC 65219-080 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namegadoterate meglumine
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215304
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsGADOTERATE MEGLUMINE (376.9 mg/mL)
Marketing started20220620
Package count1

External sources

Source: openFDA. Public-domain (CC0).