FdaApplication
NDA 208259
Identifiers
- fda_app_no: NDA208259
Properties
| Property | Value |
|---|---|
| applicant_name | ALCON LABORATORIES INC |
| application_type | NDA |
| approval_date | 2019-03-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ROCKLATAN | LATANOPROST; NETARSUDIL DIMESYLATE | 0.005%;EQ 0.02% BASE | SOLUTION/DROPS;OPHTHALMIC |
1 product