RecallHawk

MULTIHANCE (GADOBENATE DIMEGLUMINE)

BRACCO

Summary

FDA approved MULTIHANCE (GADOBENATE DIMEGLUMINE) by BRACCO. NDA (New Drug) approval (Labeling) on 2025-03-05. INJECTABLE, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA021358-26

Action Date

2025-03-05

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

MULTIHANCE (generic: GADOBENATE DIMEGLUMINE), INJECTABLE, INTRAVENOUS. Application: NDA021358

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 "NDA021358-26" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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