FdaApplication
NDA 207795
Identifiers
- fda_app_no: NDA207795
Properties
| Property | Value |
|---|---|
| applicant_name | BAUSCH AND LOMB INC |
| application_type | NDA |
| approval_date | 2017-11-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VYZULTA | LATANOPROSTENE BUNOD | 0.024% | SOLUTION/DROPS;OPHTHALMIC |
1 product