FdaApplication
NDA 020474
Identifiers
- fda_app_no: NDA020474
Properties
| Property | Value |
|---|---|
| applicant_name | HARROW EYE LLC |
| application_type | NDA |
| approval_date | 1994-12-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VEXOL | RIMEXOLONE | 1% | SUSPENSION/DROPS;OPHTHALMIC |
1 product