FdaApplication
ANDA 090423
Identifiers
- fda_app_no: ANDA090423
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2012-05-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZELASTINE HYDROCHLORIDE | AZELASTINE HYDROCHLORIDE | 0.137MG/SPRAY | SPRAY, METERED;NASAL |
1 product