United States · FDA National Drug Code directory
Naloxone Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50090-5908_fefa320d-95d8-414e-ad54-40c9f6d2c55d
- Product NDC
- 50090-5908
- Form
- INHALANT
- Composition / generic term
- Naloxone Hydrochloride Nasal
- Labeler
- A-S Medication Solutions
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20211220
- Source listing expiry
- 20261231
Source-listed ingredients
- NALOXONE HYDROCHLORIDE — 4 mg/.1mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 VIAL, SINGLE-DOSE in 1 CARTON (50090-5908-0) / .1 mL in 1 VIAL, SINGLE-DOSE · 50090-5908-0
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →