FdaApplication
ANDA 078621
Identifiers
- fda_app_no: ANDA078621
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2009-08-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZELASTINE HYDROCHLORIDE | AZELASTINE HYDROCHLORIDE | 0.05% | SOLUTION/DROPS;OPHTHALMIC |
1 product