Orange Book product
DOXORUBICIN HYDROCHLORIDE 200MG/100ML
Orange Book ANDA 064140 · TEVA PHARMACEUTICALS USA · Discontinued
Key facts
| Proprietary name | DOXORUBICIN HYDROCHLORIDE |
|---|---|
| Active ingredients | DOXORUBICIN HYDROCHLORIDE |
| Strength | 200MG/100ML |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Application | ANDA064140 |
| Applicant holder | TEVA PHARMACEUTICALS USA |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jul 28, 1995 |
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.