Ilumya

Active Ingredient(s): Tildrakizumab-asmn
FDA Approved: * March 20, 2018
Pharm Company: * MERCK SHARP DOHME
Category: Immune System

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Ilumya Overview

Tildrakizumab (trade name Ilumya (USA)/Ilumetri (European Union)) is a monoclonal antibody designed for the treatment of immunologically mediated inflammatory disorders.[1] It is approved for the treatment of adult patients with moderate-to-severe plaque psoriasis in the United States and the European Union.[2][3][4] Tildrakizumab was designed to block interleukin-23 (IL-23), a cytokine that plays a key role in managing the immu...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Tildrakizumab

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Possible Dosages for this and Related Drugs:

NDC Database Records for Ilumya: (1 result)

Sorted by National Drug Code

• 47335-177 Ilumya 100 mg/ml Subcutaneous Injection, Solution by Sun Pharma Global Fze

Other drugs which contain Tildrakizumab-asmn or a similar ingredient: (1 result)

• TILDRAKIZUMAB