OMNIPAQUE (IOHEXOL)
Summary
FDA approved OMNIPAQUE (IOHEXOL) by GE HEALTHCARE. NDA (New Drug) approval (Labeling) on 2024-10-08. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
NDA018956-119
Action Date
2024-10-08
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
OMNIPAQUE (generic: IOHEXOL), INJECTABLE, INJECTION. Application: NDA018956
Company
Context & Analysis
GE HEALTHCARE has 32 FDA actions in our database, including 18 recalls and 9 clearances.
Frequently Asked Questions
How often does GE HEALTHCARE have FDA actions?
GE HEALTHCARE has 32 FDA actions in our database, including 18 recalls and 9 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA018956-119" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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