United States · FDA National Drug Code directory
Fexinidazole
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0024-4512_1b3dbe65-328a-450b-bc3d-0b46d9acd832
- Product NDC
- 0024-4512
- Form
- TABLET
- Composition / generic term
- Fexinidazole
- Labeler
- Sanofi-Aventis U.S. LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20210716
- Source listing expiry
- 20261231
Source-listed ingredients
- FEXINIDAZOLE — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET in 1 DOSE PACK (0024-4512-14) · 0024-4512-14
- 24 TABLET in 1 DOSE PACK (0024-4512-24) · 0024-4512-24
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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