# NALOXONE HYDROCHLORIDE

NDC: 51662-1544
Generic name: NALOXONE HYDROCHLORIDE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20210808

FDA application: ANDA212455

## Active ingredients

- NALOXONE HYDROCHLORIDE: .4 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1544"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1544
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c90e2d85-ed94-2c00-e053-2a95a90ad2a0