Drug application
REVEX (NALMEFENE HYDROCHLORIDE)
Drugs@FDA NDA 020459 · HIKMA PHARMS
Key facts
| Drug name | REVEX |
|---|---|
| Active ingredients | NALMEFENE HYDROCHLORIDE |
| Application type | NDA |
| Application number | 020459 |
| Company | HIKMA PHARMS |
| Dosage forms | SOLUTION, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS |
| Strength | EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Marketing status | Discontinued |
| Reference listed drug | Yes |
| Latest submission class | Type 1 - New Molecular Entity |
| Latest submission status date | Apr 17, 1995 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- 1–9 Label versions
- 1–9 Products
- None Therapeutic equivalents
- No FDA letters on file
- Yes FDA reviews on file
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: