FdaApplication
ANDA 076362
Identifiers
- fda_app_no: ANDA076362
Properties
| Property | Value |
|---|---|
| applicant_name | TARO PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2002-11-29 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMIODARONE HYDROCHLORIDE | AMIODARONE HYDROCHLORIDE | 400MG | TABLET;ORAL |
| AMIODARONE HYDROCHLORIDE | AMIODARONE HYDROCHLORIDE | 300MG | TABLET;ORAL |
2 products