# nalmefene hydrochloride

NDC: 82432-101
Generic name: nalmefene hydrochloride injection
Labeler / Manufacturer: Chengdu Shuode Pharmaceutical Co., Ltd
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20231115

FDA application: ANDA216007

## 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:"82432-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82432-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=22d67228-6c24-47ca-afc7-52ef279520a0