Ultomiris

Active Ingredient(s): Ravulizumab-cwvz
FDA Approved: * December 21, 2018
Pharm Company: * ALEXION PHARM

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

Ultomiris Overview

Ravulizumab (ALXN1210) (INN[1]) is a humanized monoclonal antibody designed for the treatment of paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome. This drug was developed by Alexion Pharmaceuticals, Inc.[2] It was approved by the US Food and drug administration in December 2018.[3] References ^ World Health Organization (2017). "International Nonproprietary Names for Pharmaceutical Substances (INN). Proposed INN: Li...

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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/Ravulizumab

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Possible Dosages for this and Related Drugs:

NDC Database Records for Ultomiris: (1 result)

Sorted by National Drug Code

• 25682-022 Ultomiris 300 mg/30ml Intravenous Solution, Concentrate by Alexion Pharmaceuticals Inc.

Other drugs which contain Ravulizumab-cwvz or a similar ingredient: (1 result)

• RAVULIZUMAB