FdaApplication
ANDA 074206
Identifiers
- fda_app_no: ANDA074206
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PARENTERAL MEDICINES INC |
| application_type | ANDA |
| approval_date | 1993-10-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOBUTAMINE HYDROCHLORIDE | DOBUTAMINE HYDROCHLORIDE | EQ 12.5MG BASE/ML | INJECTABLE;INJECTION |
1 product