# Naloxone Hydrochloride

NDC: 71288-814
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20260101

FDA application: ANDA214211

## 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:"71288-814"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-814
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c2daaefa-6c24-4e91-9176-61e9713069fa