Orange Book product
RUBEX 10MG/VIAL
Orange Book ANDA 062926 · BRISTOL MYERS SQUIBB CO · Discontinued
Key facts
| Proprietary name | RUBEX |
|---|---|
| Active ingredients | DOXORUBICIN HYDROCHLORIDE |
| Strength | 10MG/VIAL |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Application | ANDA062926 |
| Applicant holder | BRISTOL MYERS SQUIBB CO |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Apr 13, 1989 |
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.