FdaApplication
ANDA 218256
Identifiers
- fda_app_no: ANDA218256
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2025-06-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE ACETATE | PREDNISOLONE ACETATE | 1% | SUSPENSION/DROPS;OPHTHALMIC |
1 product