Sylvant

Active Ingredient(s): Siltuximab
FDA Approved: * April 22, 2014
Pharm Company: * JANSSEN BIOTECH
Category: Cancer

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



Sylvant Overview

Siltuximab (INN, trade name Sylvant; also known as CNTO 328, anti-IL-6 chimeric monoclonal antibody or cCLB8) is a chimeric (made from human and mouse proteins) monoclonal antibody. It binds to interleukin-6.[1][2] Siltuximab has been investigated for the treatment of neoplastic diseases:[3] metastatic renal cell cancer,[4] prostate cancer,[5] and Castleman's disease,[6][7] among ot...

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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/Siltuximab

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Possible Dosages for this and Related Drugs:

Siltuximab
  • Injection: 100mg, 400mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Sylvant: (4 results)

Sorted by National Drug Code
  • 57894-420 Sylvant 100 mg Intravenous Injection, Powder, Lyophilized, for Solution by Janssen Biotech, Inc.
  • 57894-421 Sylvant 400 mg Intravenous Injection, Powder, Lyophilized, for Solution by Janssen Biotech, Inc.
  • 73090-420 Sylvant 100 mg Intravenous Injection, Powder, for Solution by Eusa Pharma (Uk) Ltd
  • 73090-421 Sylvant 400 mg Intravenous Injection, Powder, for Solution by Eusa Pharma (Uk) Ltd

Other drugs which contain Siltuximab or a similar ingredient: (1 result)