United States · FDA National Drug Code directory
Naloxone Hydrochloride Injection, USP, Auto-Injector
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
- 60842-002_04afe7f9-83ba-4269-a6ce-3bcc61a106d8
- Product NDC
- 60842-002
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Naloxone Hydrochloride
- Labeler
- Kaleo, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20220228
- Source listing expiry
- 20261231
Source-listed ingredients
- NALOXONE HYDROCHLORIDE — 10 mg/.4mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 DOSE PACK in 1 CARTON (60842-002-02) / .4 mL in 1 DOSE PACK · 60842-002-02
Source and coverage
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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.
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