Ultomiris
Active Ingredient(s): Ravulizumab-cwvzFDA 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, sold under the brand name Ultomiris, is a humanized monoclonal antibody complement inhibitor medication designed for the treatment of paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome. It is designed to bind to and prevent the activation of Complement component 5 (C5).[3][2] In paroxysmal nocturnal hemoglobinuria, proteins known as the 'complement system', which is part of the immune system, become overactive because of a g...
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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Ravulizumab-cwvz
- Injection: 300mg/30ml(10mg/ml)
NDC Database Records for Ultomiris: (3 results)
Sorted by National Drug Code- 25682-022 Ultomiris 300 mg/30ml Intravenous Solution, Concentrate by Alexion Pharmaceuticals Inc.
- 25682-025 Ultomiris 300 mg/3ml Intravenous Solution, Concentrate by Alexion Pharmaceuticals Inc.
- 25682-028 Ultomiris 1100 mg/11ml Intravenous Solution, Concentrate by Alexion Pharmaceuticals Inc.