FdaApplication
NDA 206185
Identifiers
- fda_app_no: NDA206185
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | NDA |
| approval_date | 2018-09-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| XELPROS | LATANOPROST | 0.005% | EMULSION;OPHTHALMIC |
1 product