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These highlights do not include all the information needed to use TYRUKO® safely and effectively. See full prescribing information for TYRUKO. TYRUKO (natalizumab-sztn) injection, for intravenous useInitial U.S. Approval: 2023TYRUKO (natalizumab-sztn) is biosimilar* to TYSABRI® (natalizumab).
Medication labelWhy this: Advisory · dailymed-prescription
TYRUKO is indicated as monotherapy for the treatment of relapsing forms of multiple sclerosis, to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults. Natalizumab products increase the risk of PML [see Warnings and Precautions (5.1)]. When initiating and continuing treatment with TYRUKO, physicians should consider whether the expected benefit of TYRUKO is sufficient to offset this risk. TYRUKO is indicated for inducing and maintaining clinical response and remission in adult patients with moderately to severely active Crohn’s disease with evidence of inflammation who have had an inadequate response to, or are unable to tolerate, conventional CD therapies and inhibitors of TNF-α. TYRUKO should not be used in combination with immunosuppressants (e.g., 6-mercaptopurine, azathioprine, cyclosporine, or methotrexate) or inhibitors of TNF-α [see Warnings and Precautions (5.1)].
- generic_name
- natalizumab-sztn
- product_names
- natalizumab-sztn
- ndc
- 61314-543, 61314-543-94
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en