FdaApplication
ANDA 065034
Identifiers
- fda_app_no: ANDA065034
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2001-11-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DAUNORUBICIN HYDROCHLORIDE | DAUNORUBICIN HYDROCHLORIDE | EQ 5MG BASE/VIAL | INJECTABLE;INJECTION |
1 product