DOXORUBICIN HYDROCHLORIDE
| Brand name | DOXORUBICIN HYDROCHLORIDE (LIPOSOMAL) |
|---|---|
| Active ingredient | DOXORUBICIN HYDROCHLORIDE |
| Strength | 50MG/25ML (2MG/ML) |
| Dosage form | INJECTABLE, LIPOSOMAL |
| Route | INJECTION |
| Modality | Small molecule |
| FDA approval | July 2024 |
| 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.