# NALMEFENE HYDROCHLORIDE

NDC: 59011-960
Generic name: NALMEFENE HYDROCHLORIDE
Labeler / Manufacturer: Knoa Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20220208

FDA application: ANDA212955

## Active ingredients

- NALMEFENE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59011-960"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59011-960
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3abfbffc-9e52-4fc6-ae92-6e0a97f4afe7