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] In the United States, it is approved for the treatment of moderate-to-severe plaque psoriasis.[2] Tildrakizumab was designed to block interleukin-23, a cytokine that plays an important role in managing the immune system and autoimmune disease. Contents 1 History 2 Approvals and indicati...

Read more Ilumya Details
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