FdaApplication
ANDA 070364
Identifiers
- fda_app_no: ANDA070364
Properties
| Property | Value |
|---|---|
| applicant_name | ABRAXIS PHARMACEUTICAL PRODUCTS |
| application_type | ANDA |
| approval_date | 1985-12-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOPAMINE HYDROCHLORIDE | DOPAMINE HYDROCHLORIDE | 160MG/ML | INJECTABLE;INJECTION |
1 product