Drug application
CERUBIDINE (DAUNORUBICIN HYDROCHLORIDE)
Drugs@FDA NDA 050484 · WYETH AYERST
Key facts
| Drug name | CERUBIDINE |
|---|---|
| Active ingredients | DAUNORUBICIN HYDROCHLORIDE |
| Application type | NDA |
| Application number | 050484 |
| Company | WYETH AYERST |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | EQ 20MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 1 - New Molecular Entity |
| Latest submission status date | Dec 19, 1979 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.