NDC 63020-198

Alunbrig 90 mg / 180 mg kit

On the label: Takeda Pharmaceuticals America, Inc..

United States: 2Belgium: 1United Kingdom: 1Ireland: 1

Where it's made

FactoryWhereRoleLast FDA inspection
AMPAC Fine Chemicals LLCRancho Cordova, CA, United StatesMakes the active ingredient and tests it No problems foundSep 10, 2025 · 9 inspections, 1 with FDA action
Ajinomoto OmnichemWetteren, BelgiumMakes the active ingredient and tests it Problems found, fixed voluntarilyJun 13, 2025 · 5 inspections
Curia New York, Inc.Rensselaer, NY, United StatesMakes the active ingredient and tests it Serious problems, FDA actionFeb 5, 2026 · 8 inspections, 1 with FDA action
Penn Pharmaceutical Services LimitedTredegar, United KingdomMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyApr 1, 2022 · 6 inspections
Takeda Ireland LimitedBray, IrelandMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyDec 9, 2022 · 6 inspections
Almac Sciences (Ireland) LimitedAthlone, IrelandTests it Problems found, fixed voluntarilyJan 29, 2025 · 4 inspections
Solvias AGKaiseraugst, SwitzerlandTests it Problems found, fixed voluntarilyAug 7, 2025 · 10 inspections

Product details

Generic drug
Brigatinib: every company that makes it
Form
kit
Strength
90 mg / 180 mg
Approval
NDA NDA208772
On the market since
Apr 28, 2017
Package NDCs
63020-090-07 63020-180-23 63020-198-30
Official label
DailyMed (National Library of Medicine), updated Jan 12, 2026

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