FdaApplication
ANDA 211526
Identifiers
- fda_app_no: ANDA211526
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2021-11-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIFLUPREDNATE | DIFLUPREDNATE | 0.05% | EMULSION;OPHTHALMIC |
1 product