FdaApplication
ANDA 074739
Identifiers
- fda_app_no: ANDA074739
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA |
| application_type | ANDA |
| approval_date | 1998-11-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMIODARONE HYDROCHLORIDE | AMIODARONE HYDROCHLORIDE | 200MG | TABLET;ORAL |
1 product