NDC 63020-090
Alunbrig 90 mg tablet, film coated
On the label: Takeda Pharmaceuticals America, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| AMPAC Fine Chemicals LLC | Rancho Cordova, CA, United States | Makes the active ingredient and tests it | No problems foundSep 10, 2025 · 9 inspections, 1 with FDA action |
| Ajinomoto Omnichem | Wetteren, Belgium | Makes the active ingredient and tests it | Problems found, fixed voluntarilyJun 13, 2025 · 5 inspections |
| Curia New York, Inc. | Rensselaer, NY, United States | Makes the active ingredient and tests it | Serious problems, FDA actionFeb 5, 2026 · 8 inspections, 1 with FDA action |
| Penn Pharmaceutical Services Limited | Tredegar, United Kingdom | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 1, 2022 · 6 inspections |
| Takeda Ireland Limited | Bray, Ireland | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyDec 9, 2022 · 6 inspections |
| Almac Sciences (Ireland) Limited | Athlone, Ireland | Tests it | Problems found, fixed voluntarilyJan 29, 2025 · 4 inspections |
| Solvias AG | Kaiseraugst, Switzerland | Tests it | Problems found, fixed voluntarilyAug 7, 2025 · 10 inspections |
Product details
- Generic drug
- Brigatinib: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 90 mg
- Approval
- NDA NDA208772
- On the market since
- Apr 28, 2017
- Package NDCs
63020-090-0763020-090-30- Official label
- DailyMed (National Library of Medicine), updated Jan 12, 2026
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