In the US, Ibrutinib (ibrutinib systemic) is a member of the drug class multikinase inhibitors and is used to treat Chronic Lymphocytic Leukemia, Graft-versus-host disease, Lymphoma, Mantle Cell Lymphoma, Non-Hodgkin's Lymphoma and Waldenström Macroglobulinemia.
ATC (Anatomical Therapeutic Chemical Classification)
CAS registry number (Chemical Abstracts Service)
Antineoplastic agent: Tyrosine kinase inhibitor
- Ibrutinibum (Latin)
- Ibrutinib (German)
- Ibrutinib (French)
- Ibrutinib (Spanish)
- Ibrutinib (OS: USAN, JAN)
- UNII-1X70OSD4VX (IS)
- Ibrutinib (PH: JP XVI)
Catalent CTS, Israel; Janssen, Canada; Janssen, Denmark; Janssen, Ireland; Janssen, Norway; Janssen, New Zealand; Janssen, Sweden; Janssen, Slovakia; Janssen Cilag, Argentina; Janssen Pharmaceutica, Belgium; Janssen Pharmaceutical, Japan; Janssen-Cilag, Australia; Janssen-Cilag, Bosnia & Herzegowina; Janssen-Cilag, Brazil; Janssen-Cilag, Colombia; Janssen-Cilag, Czech Republic; Janssen-Cilag, Germany; Janssen-Cilag, Spain; Janssen-Cilag, United Kingdom; Janssen-Cilag, Greece; Janssen-Cilag, Lithuania; Janssen-Cilag, Peru; Janssen-Cilag, Poland; Janssen-Cilag International, Iceland; Janssen-Cilag International, Romania; Janssen-Cilag International NV, Netherlands; Janssen-Cilag International NV, Slovenia; Johnson & Johnson, Croatia (Hrvatska); Johnson & Johnson, Turkey; Pharmacyclics, China; Pharmacyclics, United States
- Imbruvica 140mg
Janssen, Hungary; Janssen, Luxembourg; Janssen-Cilag, Switzerland; Janssen-Cilag Pharma, Austria
|JAN||Japanese Accepted Name|
|Rec.INN||Recommended International Nonproprietary Name (World Health Organization)|
|USAN||United States Adopted Name|
|WHO||World Health Organization|
Further information on drug naming conventions: International Nonproprietary Names.
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