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
- 60219-2104_a79738c5-1989-43c7-856b-f284c654c9c0
- Product NDC
- 60219-2104
- Form
- SPRAY
- Composition / generic term
- Naloxone
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240424
- Source listing expiry
- 20271231
Source-listed ingredients
- NALOXONE HYDROCHLORIDE — 4 mg/.1mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 VIAL in 1 CARTON (60219-2104-7) / .1 mL in 1 VIAL (60219-2104-1) · 60219-2104-7
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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