FdaApplication
NDA 211039
Identifiers
- fda_app_no: NDA211039
Properties
| Property | Value |
|---|---|
| applicant_name | BAUSCH AND LOMB IRELAND LTD |
| application_type | NDA |
| approval_date | 2020-03-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLUORESCEIN SODIUM AND BENOXINATE HYDROCHLORIDE | BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM | 0.4%;0.3% | SOLUTION/DROPS;OPHTHALMIC |
1 product