FdaApplication
ANDA 070059
Identifiers
- fda_app_no: ANDA070059
Properties
| Property | Value |
|---|---|
| applicant_name | ABRAXIS PHARMACEUTICAL PRODUCTS |
| application_type | ANDA |
| approval_date | 1985-03-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOPAMINE HYDROCHLORIDE | DOPAMINE HYDROCHLORIDE | 80MG/ML | INJECTABLE;INJECTION |
1 product