FdaApplication
ANDA 076601
Identifiers
- fda_app_no: ANDA076601
Properties
| Property | Value |
|---|---|
| applicant_name | TARO PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2008-06-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CETIRIZINE HYDROCHLORIDE | CETIRIZINE HYDROCHLORIDE | 5MG/5ML | SOLUTION;ORAL |
1 product