Nucala

Active Ingredient(s): Mepolizumab
FDA Approved: * November 4, 2015
Pharm Company: * GLAXOSMITHKLINE LLC
Category: Asthma

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



Nucala Overview

Mepolizumab (trade name Nucala) is a humanized monoclonal antibody used for the treatment of severe eosinophilic asthma. It recognizes and blocks interleukin-5 (IL-5), a signalling protein of the immune system. Contents 1 Medical uses 2 Side effects 3 Overdose 4 Interactions 5 Pharmacology 5.1 Mechanism of action 5.2 Pharmacokinetics 6 Chemistry 7 History 8 Research 9 References Medical uses Mepolizumab is approved by the U.S. Food and Drug Administration (FDA) for the maintenance...

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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/Mepolizumab

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Possible Dosages for this and Related Drugs:

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

NDC Database Records for Nucala: (3 results)

Sorted by National Drug Code
  • 0173-0881 Nucala 100 mg/ml Subcutaneous Injection, Powder, for Solution by Glaxosmithkline LLC
  • 0173-0892 Nucala 100 mg/ml Subcutaneous Injection, Solution by Glaxosmithkline LLC
  • 12064-018 Nucala 100 mg/ml Subcutaneous Injection, Powder, for Solution by Glaxosmithkline Manufacturing Spa

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




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