Data / Drug companies / Naloxone hydrochloride nasal
Naloxone hydrochloride nasal: 3 companies and 3 products in the FDA NDC directory
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Naloxone hydrochloride nasal is listed in the FDA National Drug Code Directory by 3 companies, with 3 products in commercial distribution. 0 of the products (0.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are spray; inhalant, and the newest product started marketing on August 28, 2023.
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- Companies listing it
- 3
- Products
- 3
- Generic (ANDA) products
- 0 (0.0%)
- Application numbers
- 1
- Routes
- Nasal
- Brand names
- Narcan, Naloxone Hydrochloride
- openFDA record search
- api.fda.gov
Companies that list naloxone hydrochloride nasal
Ranked by number of products. Finished drugs in commercial distribution.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 1 | inhalant | Authorized generics (NDA) | December 20, 2021 |
| Emergent Devices Inc. | 1 | spray | New drug applications (NDA) | August 28, 2023 |
| Sportpharm LLC | 1 | spray | New drug applications (NDA) | August 28, 2023 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Spray | 2 | 66.7% |
| Inhalant | 1 | 33.3% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 2 | 66.7% |
| Authorized generics (NDA) | 1 | 33.3% |
Pharmacologic classes
| Class | Products |
|---|---|
| Opioid Antagonist | 3 |
CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.