# Naloxone Hydrochloride

NDC: 67457-992
Generic name: Naloxone Hydrochloride
Labeler / Manufacturer: Mylan Institutional LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20221202

FDA application: ANDA213843

## 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:"67457-992"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67457-992
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7faaedb3-227b-408d-b772-6b326638b00e