FdaApplication
ANDA 216935
Identifiers
- fda_app_no: ANDA216935
Properties
| Property | Value |
|---|---|
| applicant_name | LUPIN LTD |
| application_type | ANDA |
| approval_date | 2024-08-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE ACETATE | PREDNISOLONE ACETATE | 1% | SUSPENSION/DROPS;OPHTHALMIC |
1 product