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Brukinsa — Description, Dosage, Side Effects | PillsCard
OTC
Brukinsa
INN: zanubrutinib
Data updated: 2026-05-02
Available in:
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About This Product
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Manufacturer
BeOne Medicines Ireland Limited
ATC Code
L01EL03
Source
EMA · EMEA/H/C/004978
USDailyMed:Zanubrutinib
AU:D
L01EL03(WHO)
AU:S4(Prescription only)CA:℞-onlyUS:℞-onlyEU:Rx-onlyRx-only
1691249-45-2
135565884
DB15035
64835237
AG9MHG098Z
D11422
ChEMBL3936761
BA0 (PDBe,RCSB PDB)
Interactive image
NC(=O)C1=C2NCC[C@@H](C3CCN(CC3)C(=O)C=C)N2N=C1C1=CC=C(OC2=CC=CC=C2)C=C1
InChI=1S/C27H29N5O3/c1-2-23(33)31-16-13-18(14-17-31)22-12-15-29-27-24(26(28)34)25(30-32(22)27)19-8-10-21(11-9-19)35-20-6-4-3-5-7-20/h2-11,18,22,29H,1,12-17H2,(H2,28,34)/t22-/m0/s1Key:RNOAOAWBMHREKO-QFIPXVFZSA-N
Zanubrutinib, sold under the brand nameBrukinsa, is ananticancer medicationused for the treatment ofmantle cell lymphoma(MCL),Waldenström's macroglobulinemia(WM),marginal zone lymphoma(MZL), andchronic lymphocytic leukemia(CLL).Zanubrutinib is classified as aBruton's tyrosine kinase(BTK) inhibitor.It is givenby mouth.
It was approved for medical use in the United States in November 2019.Zanubrutinib is a therapeutic alternative on theWorld Health Organization's List of Essential Medicines.