NDC 0024-5908

Kevzara 150 mg per 1.14 mL injection, solution

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

Ireland: 1United States: 1France: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Genzyme Ireland LimitedWaterford, IrelandMakes it and tests it Problems found, fixed voluntarilyFeb 25, 2022 · 7 inspections
Regeneron Pharmaceuticals, Inc.Rensselaer, NY, United StatesMakes it, makes the active ingredient and tests it Problems found, fixed voluntarilyMar 22, 2024 · 10 inspections
Sanofi Winthrop IndustrieLe Trait, FranceMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyApr 25, 2023 · 6 inspections
Genzyme CorporationNorthborough, MA, United StatesPackages it and labels it No problems foundAug 14, 2025 · 6 inspections
Nelson Laboratories, LLCSalt Lake City, UT, United StatesTests it Problems found, fixed voluntarilyJun 2, 2023 · 6 inspections

Product details

Generic drug
Sarilumab: every company that makes it
Form
injection, solution, subcutaneous
Strength
150 mg per 1.14 mL
Approval
BLA BLA761037
On the market since
May 22, 2017
Package NDCs
0024-5908-00 0024-5908-01 0024-5908-02
Official label
DailyMed (National Library of Medicine), updated Feb 27, 2026

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