# Gadoterate Meglumine

NDC: 65219-088
Generic name: gadoterate meglumine
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20220620

FDA application: ANDA215982

## Active ingredients

- GADOTERATE MEGLUMINE: 376.9 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-088"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-088
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fbebe7f2-a0c2-4fd5-b421-8fbcbaf46709