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
- 71205-707_8d529b4c-85fd-4e50-9443-9080825307bf
- Product NDC
- 71205-707
- Form
- SPRAY
- Composition / generic term
- naloxone hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220621
- 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 (71205-707-02) / .1 mL in 1 VIAL, SINGLE-DOSE · 71205-707-02
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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