Drug application
NALOXONE HYDROCHLORIDE (NALOXONE HYDROCHLORIDE)
Drugs@FDA ANDA 211951 · PADAGIS ISRAEL
Key facts
| Drug name | NALOXONE HYDROCHLORIDE |
|---|---|
| Active ingredients | NALOXONE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 211951 |
| Company | PADAGIS ISRAEL |
| Dosage forms | SPRAY, METERED, NASAL |
| Strength | 4MG/SPRAY |
| Marketing status | Over-the-counter |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Jun 21, 2022 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
- Yes FDA letters on file
- No 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: