# Zurnai

NDC: 59011-962
Generic name: NALMEFENE HYDROCHLORIDE
Labeler / Manufacturer: Knoa Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, SUBCUTANEOUS
Marketing started: 20250807

FDA application: NDA218590

## Active ingredients

- NALMEFENE HYDROCHLORIDE: 1.5 mg/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59011-962"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59011-962
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a59a5847-9fe4-4341-a203-be0a5e6d3e36