FdaApplication
ANDA 091626
Identifiers
- fda_app_no: ANDA091626
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2011-10-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EPINASTINE HYDROCHLORIDE | EPINASTINE HYDROCHLORIDE | 0.05% | SOLUTION/DROPS;OPHTHALMIC |
1 product