FdaApplication
ANDA 065000
Identifiers
- fda_app_no: ANDA065000
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 1999-05-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DAUNORUBICIN HYDROCHLORIDE | DAUNORUBICIN HYDROCHLORIDE | EQ 20MG BASE/VIAL | INJECTABLE;INJECTION |
1 product