IOHEXOL
Summary
FDA approved IOHEXOL by AMNEAL. ANDA (Generic) approval (Manufacturing (CMC)) on 2026-06-25. SOLUTION, INJECTION, ORAL, RECTAL.
Details
Source
Drug Approval
External ID
ANDA217737-1
Action Date
2026-06-25
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
IOHEXOL, SOLUTION, INJECTION, ORAL, RECTAL. Application: ANDA217737
Company
Context & Analysis
AMNEAL has 70 FDA actions in our database.
Frequently Asked Questions
How often does AMNEAL have FDA actions?
AMNEAL has 70 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 "ANDA217737-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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