# IOMERVU

NDC: 0270-7018
Generic name: Iomeprol Injection
Labeler / Manufacturer: BRACCO DIAGNOSTICS INC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRA-ARTERIAL, INTRAVENOUS
Marketing started: 20260101

FDA application: NDA216016

## Active ingredients

- IOMEPROL: 816 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0270-7018"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0270-7018
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb2e0e00-7c93-0fb4-89a5-861641662a5a