Orange Book product
DOXORUBICIN HYDROCHLORIDE 50MG/VIAL
Orange Book ANDA 208888 · AMNEAL EU LTD · Prescription
Key facts
| Proprietary name | DOXORUBICIN HYDROCHLORIDE |
|---|---|
| Active ingredients | DOXORUBICIN HYDROCHLORIDE |
| Strength | 50MG/VIAL |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Application | ANDA208888 |
| Applicant holder | AMNEAL EU LTD |
| Marketing status | Prescription |
| Therapeutic equivalence (TE) code | AP |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Feb 17, 2017 |
At a glance
- 1–9 Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.