FdaApplication
ANDA 073000
Identifiers
- fda_app_no: ANDA073000
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PARENTERAL MEDICINES INC |
| application_type | ANDA |
| approval_date | 1991-10-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOPAMINE HYDROCHLORIDE | DOPAMINE HYDROCHLORIDE | 80MG/ML | INJECTABLE;INJECTION |
1 product