# Naloxone Hydrochloride

NDC: 42023-224
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20241105

FDA application: ANDA215964

## Active ingredients

- NALOXONE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42023-224"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-224
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3ae08e26-223b-4971-b2f1-f1e183a3f930