FdaApplication
ANDA 090229
Identifiers
- fda_app_no: ANDA090229
Properties
| Property | Value |
|---|---|
| applicant_name | SYNTHON BV |
| application_type | ANDA |
| approval_date | 2010-11-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LEVOCETIRIZINE DIHYDROCHLORIDE | LEVOCETIRIZINE DIHYDROCHLORIDE | 5MG | TABLET;ORAL |
1 product