# Naloxone Hydrochloride Injection, USP, Auto-Injector

NDC: 60842-002
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: Kaleo, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, SUBCUTANEOUS
Marketing started: 20220228

FDA application: NDA215457

## Active ingredients

- NALOXONE HYDROCHLORIDE: 10 mg/.4mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60842-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60842-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b5463553-b775-47a3-8d10-31e01ca1ec72