FdaApplication
NDA 021664
Identifiers
- fda_app_no: NDA021664
Properties
| Property | Value |
|---|---|
| applicant_name | BAUSCH AND LOMB INC |
| application_type | NDA |
| approval_date | 2005-03-24 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BROMDAY | BROMFENAC SODIUM | EQ 0.09% ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION/DROPS;OPHTHALMIC |
| XIBROM | BROMFENAC SODIUM | EQ 0.09% ACID **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION/DROPS;OPHTHALMIC |
2 products