FdaApplication
ANDA 077555
Identifiers
- fda_app_no: ANDA077555
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2011-11-04 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TIAGABINE HYDROCHLORIDE | TIAGABINE HYDROCHLORIDE | 4MG | TABLET;ORAL |
| TIAGABINE HYDROCHLORIDE | TIAGABINE HYDROCHLORIDE | 2MG | TABLET;ORAL |
2 products