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
- 55150-345_6b48182a-4a21-4157-8efb-591ee87fb7d6
- Product NDC
- 55150-345
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Naloxone Hydrochloride
- Labeler
- Eugia US LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210114
- Source listing expiry
- 20261231
Source-listed ingredients
- NALOXONE HYDROCHLORIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 SYRINGE in 1 BOX (55150-345-01) / 2 mL in 1 SYRINGE · 55150-345-01
- 10 SYRINGE in 1 BOX (55150-345-10) / 2 mL in 1 SYRINGE · 55150-345-10
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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