IOMERVU (IOMEPROL INJECTION)
Summary
FDA approved IOMERVU (IOMEPROL INJECTION) by BRACCO. NDA (New Drug) approval (Type 1 - New Molecular Entity) on 2024-11-27. SOLUTION, INTRA-ARTERIAL.
Details
Source
Drug Approval
External ID
NDA216016-1
Action Date
2024-11-27
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
IOMERVU (generic: IOMEPROL INJECTION), SOLUTION, INTRA-ARTERIAL. Application: NDA216016
Company
Context & Analysis
BRACCO has 7 FDA actions in our database.
Frequently Asked Questions
How often does BRACCO have FDA actions?
BRACCO has 7 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA216016-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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