FdaApplication
ANDA 220360
Identifiers
- fda_app_no: ANDA220360
Properties
| Property | Value |
|---|---|
| applicant_name | MANKIND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2025-12-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LATANOPROST | LATANOPROST | 0.005% | SOLUTION/DROPS;OPHTHALMIC |
1 product