FdaApplication
ANDA 062926
Identifiers
- fda_app_no: ANDA062926
Properties
| Property | Value |
|---|---|
| applicant_name | BRISTOL MYERS SQUIBB CO |
| application_type | ANDA |
| approval_date | 1989-04-13 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| RUBEX | DOXORUBICIN HYDROCHLORIDE | 10MG/VIAL | INJECTABLE;INJECTION |
| RUBEX | DOXORUBICIN HYDROCHLORIDE | 100MG/VIAL | INJECTABLE;INJECTION |
| RUBEX | DOXORUBICIN HYDROCHLORIDE | 50MG/VIAL | INJECTABLE;INJECTION |
3 products