Active Ingredient(s): Emicizumab
FDA Approved: * November 16, 2017
Pharm Company: * GENENTECH INC
Category: Blood Clotting (Hemostasis)

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

Hemlibra Overview

Emicizumab (trade name Hemlibra) is a humanized monoclonal antibody for the treatment of haemophilia A, developed by Chugai (a subsidiary of Roche).[1] A Phase I clinical trial found that it was well tolerated by healthy subjects.[2] In November 2017, it was approved by the US FDA.[3] Mechanism of action Emicizumab binds to both the activated coagulation factor IX and to factor X, mediating the activation of the latter. This is normally the function of coagulation factor VIII, which is miss...

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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/Emicizumab

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Possible Dosages for this and Related Drugs:

  • Injection: 105mg/0.7ml, 150mg, 30mg/ml, 60mg/0.4ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Hemlibra: (4 results)

Sorted by National Drug Code
  • 50242-920 Hemlibra 30 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
  • 50242-921 Hemlibra 150 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
  • 50242-922 Hemlibra 150 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
  • 50242-923 Hemlibra 150 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.

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

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