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 indicat...

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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:

Tildrakizumab-asmn
  • Injection: 100mg/1ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

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)






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