Quick answers
- What is Narcan Naloxone Hci?
- Narcan Naloxone Hci is a brand name of Naloxone hydrochloride, a prescription medicine. The FDA NDC Directory lists 1 Narcan Naloxone Hci product in 1 strength and form.
- Who makes Narcan Naloxone Hci?
- Emergent holds the FDA application for Narcan Naloxone Hci (NDA208411, approved November 18, 2015).
- Is there a generic or store brand of Narcan Naloxone Hci?
- Yes. The FDA NDC Directory lists 6 other products with the same active ingredients, strength and form as a Narcan Naloxone Hci product, 3 of them generic. Ask your pharmacist whether one is right for you.
- Has Narcan Naloxone Hci been recalled?
- No recall linked to Narcan Naloxone Hci products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Narcan Naloxone Hci is
Each Narcan Naloxone Hci product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Naloxone hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| naloxone hydrochloride 4 mg/0.1 mL spray (nasal) | Narcan Naloxone Hci | 6 products, 4 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Naloxone hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA208411 | Emergent | November 18, 2015 | 1 |
Companies that list Narcan Naloxone Hci
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Narcan Naloxone Hci products.
Recalls
No recall linked to Narcan Naloxone Hci products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.