FdaApplication
ANDA 077234
Identifiers
- fda_app_no: ANDA077234
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA FARMACEUTICA (PORTUGAL) SA |
| application_type | ANDA |
| approval_date | 2008-02-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMIODARONE HYDROCHLORIDE | AMIODARONE HYDROCHLORIDE | 50MG/ML | INJECTABLE;INJECTION |
1 product