NDC 78670-150

iwilfin 250 mg tablet

On the label: Uswm, LLC.

United States: 2Taiwan: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Corerx, Inc.Clearwater, FL, United StatesMakes it and tests it Problems found, fixed voluntarilyFeb 26, 2026 · 5 inspections
Corerx, Inc.Clearwater, FL, United StatesMakes it Problems found, fixed voluntarilyFeb 26, 2026 · 5 inspections
ScinoPharm Taiwan, Ltd.Tainan, TaiwanMakes the active ingredient, tests it and packages it Serious problems, FDA actionJun 23, 2026 · 7 inspections, 1 with FDA action
Aphena Pharma Solutions - Tennessee, LLCCookeville, TN, United StatesPackages it and labels it No problems foundJul 25, 2022 · 11 inspections
Quality Chemical LaboratoriesWilmington, NC, United StatesTests it Problems found, fixed voluntarilyNov 20, 2024 · 5 inspections
SGS North America Inc.Fairfield, NJ, United StatesTests it Problems found, fixed voluntarilyJun 9, 2026 · 8 inspections

Product details

Generic drug
Eflornithine: every company that makes it
Form
tablet, oral
Strength
250 mg
Approval
NDA NDA215500
On the market since
Jan 15, 2024
Package NDCs
78670-150-01
Official label
DailyMed (National Library of Medicine), updated Mar 26, 2026

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