FdaApplication
ANDA 064212
Identifiers
- fda_app_no: ANDA064212
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PARENTERAL MEDICINES INC |
| application_type | ANDA |
| approval_date | 1998-06-23 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DAUNORUBICIN HYDROCHLORIDE | DAUNORUBICIN HYDROCHLORIDE | EQ 50MG BASE/VIAL | INJECTABLE;INJECTION |
| DAUNORUBICIN HYDROCHLORIDE | DAUNORUBICIN HYDROCHLORIDE | EQ 20MG BASE/VIAL | INJECTABLE;INJECTION |
2 products