# NALOXONE HCl

NDC: 51662-1620
Generic name: NALOXONE HCl
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20230410

FDA application: ANDA211951

## Active ingredients

- NALOXONE HYDROCHLORIDE: 4 mg/.1mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1620"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1620
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f8fcda15-8ba6-e66a-e053-6294a90a385c