FdaApplication
NDA 203168
Identifiers
- fda_app_no: NDA203168
Properties
| Property | Value |
|---|---|
| applicant_name | BAUSCH AND LOMB INC |
| application_type | NDA |
| approval_date | 2013-04-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROLENSA | BROMFENAC SODIUM | EQ 0.07% ACID | SOLUTION/DROPS;OPHTHALMIC |
1 product