# Naloxone Hydrochloride

NDC: 55150-327
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: Eugia US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20191015

FDA application: ANDA212455

## Active ingredients

- NALOXONE HYDROCHLORIDE: .4 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55150-327"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55150-327
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c7fa8d4f-28a7-4ef5-aef8-cbd4328ce599