# Naloxone Hydrochloride

NDC: 76329-3469
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: International Medication Systems, Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: PARENTERAL
Marketing started: 20160728

FDA application: ANDA072076

## 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:"76329-3469"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76329-3469
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d2f5bfa0-933e-46d0-8b1a-9f90e6aaba54