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
- 72572-450_8d5154a2-b3a7-4f1c-9ac8-af8c21f21e96
- Product NDC
- 72572-450
- Form
- INJECTION
- Composition / generic term
- Nalxone Hydrochloride
- Labeler
- Civica, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191111
- Source listing expiry
- 20271231
Source-listed ingredients
- NALOXONE HYDROCHLORIDE — .4 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (72572-450-25) / 1 mL in 1 VIAL (72572-450-01) · 72572-450-25
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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