Naloxone Hydrochloride
- Product NDC
- 50090-5908
- 11-digit product format
- 500905908
- Labeler code
- 50090
- Product ID
- 50090-5908_fefa320d-95d8-414e-ad54-40c9f6d2c55d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naloxone Hydrochloride Nasal
- Dosage form
- INHALANT
- Route
- NASAL
- Labeler
- A-S Medication Solutions
- Application
- NDA208411
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-12-20
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- 4 mg/.1mL
- Pharmacologic classes
- Opioid Antagonist [EPC], Opioid Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F850569PQR | NALOXONE HYDROCHLORIDE | 357-08-4 | NALOXONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-5908-0 | 50090590800 | 2 VIAL, SINGLE-DOSE in 1 CARTON (50090-5908-0) / .1 mL in 1 VIAL, SINGLE-DOSE | 2022-01-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Naloxone Hydrochloride | A-S Medication Solutions | 2023-11-24 | HUMAN PRESCRIPTION DRUG LABEL | 3 |