Ilumya
Active Ingredient(s): Tildrakizumab-asmnFDA 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 (US)/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 immun...
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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Tildrakizumab-asmn
- Injection: 100mg/1ml
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