NDC 0024-4512

Fexinidazole 600 mg tablet

On the label: Sanofi-Aventis U.S. LLC.

United States: 1Hungary: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Alcami Carolinas CorporationWilmington, NC, United StatesMakes it Problems found, fixed voluntarilySep 26, 2025 · 11 inspections
EUROAPI Hungary Ltd.Budapest, HungaryMakes the active ingredient and tests it No problems foundJun 21, 2019 · 4 inspections
Alcami Carolinas CorporationWilmington, NC, United StatesPackages it and labels it Problems found, fixed voluntarilySep 26, 2025 · 11 inspections
Alcami Carolinas CorporationWilmington, NC, United StatesTests it Problems found, fixed voluntarilySep 26, 2025 · 11 inspections

Product details

Generic drug
Fexinidazole: every company that makes it
Form
tablet, oral
Strength
600 mg
Approval
NDA NDA214429
On the market since
Jul 16, 2021
Package NDCs
0024-4512-14 0024-4512-24
Official label
DailyMed (National Library of Medicine), updated May 2, 2025

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