# NALOXONE HYDROCHLORIDE

NDC: 0404-9922
Generic name: naloxone hydrochloride
Labeler / Manufacturer: Henry Schein, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: PARENTERAL
Marketing started: 20220113

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:"0404-9922"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0404-9922
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bd65e3fe-cd7a-4855-8f55-8cc3a0921ccc