Drug application
OXYMORPHONE HYDROCHLORIDE (OXYMORPHONE HYDROCHLORIDE)
Drugs@FDA ANDA 079046 · ACTAVIS ELIZABETH
Key facts
| Drug name | OXYMORPHONE HYDROCHLORIDE |
|---|---|
| Active ingredients | OXYMORPHONE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 079046 |
| Company | ACTAVIS ELIZABETH |
| Dosage forms | TABLET, EXTENDED RELEASE, ORAL |
| Strength | 7.5MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Jul 11, 2013 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 1–9 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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: