FdaApplication
ANDA 207606
Identifiers
- fda_app_no: ANDA207606
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2023-01-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CYCLOSPORINE | CYCLOSPORINE | 0.05% | EMULSION;OPHTHALMIC |
1 product