DAUNORUBICIN HYDROCHLORIDE
| Brand name | DAUNORUBICIN HYDROCHLORIDE |
|---|---|
| Active ingredient | DAUNORUBICIN HYDROCHLORIDE |
| Strength | EQ 20MG BASE/VIAL |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Modality | Small molecule |
| FDA approval | May 1999 |
| Marketing status | RX |
Source: FDA Orange Book, layered on the CliffBio company graph. Cliff dates are the loss of exclusivity; estimates are projections, not legal advice.