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
- 84549-072_3f2bb95a-aece-c0b7-e063-6394a90a627b
- Product NDC
- 84549-072
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Naloxone Hydrochloride
- Labeler
- ProPharma Distribution
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170726
- Source listing expiry
- 20261231
Source-listed ingredients
- NALOXONE HYDROCHLORIDE — .4 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 mL in 1 VIAL, GLASS (84549-072-10) · 84549-072-10
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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