FdaApplication
ANDA 078738
Identifiers
- fda_app_no: ANDA078738
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2010-06-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZELASTINE HYDROCHLORIDE | AZELASTINE HYDROCHLORIDE | 0.05% | SOLUTION/DROPS;OPHTHALMIC |
1 product