BRUKINSA® (Zanubrutinib) November 29, 2019April 5, 2020 RR FDA Approvals Non-Hodgkin Lymphoma The FDA on November 14, 2019 granted accelerated approval to BRUKINSA® for adult patients with Mantle Cell Lymphoma (MCL) who have received at least one prior therapy. BRUKINSA® is a product of BeiGene, Ltd. Related Posts:BRUKINSA® (Zanubrutinib)BRUKINSA® (Zanubrutinib)BRUKINSA® (Zanubrutinib)BRUKINSA® Superior to IMBRUVICA® in…BRUKINSA® Superior to IMBRUVICA® in…BRUKINSA® for First Line Treatment of Chronic…