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Fexinidazole

NDC 0024-4512 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSanofi-Aventis U.S. LLC
Marketing categoryNew Drug Application (innovator) · App NDA214429
Dosage form / routeTABLET · ORAL
Active ingredientsFEXINIDAZOLE (600 mg/1)
Marketing started20210716
Package count2

External sources

Source: openFDA. Public-domain (CC0).