FdaApplication
ANDA 217737
Identifiers
- fda_app_no: ANDA217737
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2025-11-13 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IOHEXOL | IOHEXOL | 75.5% | SOLUTION;INJECTION, ORAL |
| IOHEXOL | IOHEXOL | 64.7% | SOLUTION;INJECTION, ORAL, RECTAL |
2 products