Drug application
NARCAN (NALOXONE HYDROCHLORIDE)
Drugs@FDA ANDA 071083 · BRISTOL MYERS SQUIBB
Key facts
| Drug name | NARCAN |
|---|---|
| Active ingredients | NALOXONE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 071083 |
| Company | BRISTOL MYERS SQUIBB |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | 0.4MG/ML |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Jul 28, 1988 |
At a glance
- 1–9 Submissions
- 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.