# Fexinidazole

NDC: 0024-4512
Generic name: Fexinidazole
Labeler / Manufacturer: Sanofi-Aventis U.S. LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210716

FDA application: NDA214429

## Active ingredients

- FEXINIDAZOLE: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0024-4512"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0024-4512
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74a611bc-9977-46bb-b626-0370b3031628