# Naloxone Hydrochloride

NDC: 0409-1782
Generic name: NALOXONE HYDROCHLORIDE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20050923

FDA application: ANDA070172

## 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:"0409-1782"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-1782
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b598c237-032d-4bb5-0e92-50eabd863dac