# Naloxone Hydrochloride

NDC: 60219-2104
Generic name: Naloxone
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20240424

FDA application: ANDA217992

## Active ingredients

- NALOXONE HYDROCHLORIDE: 4 mg/.1mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60219-2104"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60219-2104
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8779a073-dc6e-410a-9959-fd370f0079f9