# KLOXXADO

NDC: 59467-679
Generic name: Naloxone HCL
Labeler / Manufacturer: Hikma Specialty USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SPRAY
Routes: NASAL
Marketing started: 20210803

FDA application: NDA212045

## Active ingredients

- NALOXONE HYDROCHLORIDE: 8 mg/.1mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59467-679"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59467-679
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ebf0f833-c1c0-487c-8f29-01fa8c61b6cb