Udenyca

Active Ingredient(s): Pegfilgrastim-cbqv
FDA Approved: * November 2, 2018
Pharm Company: * COHERUS BIOSCIENCES INC
Category: Cancer

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



Udenyca Overview

Pegfilgrastim is a PEGylated form of the recombinant human granulocyte colony-stimulating factor (GCSF) analog filgrastim. It serves to stimulate the production of white blood cells (neutrophils).[2] Pegfilgrastim treatment can be used to stimulate bone marrow to produce more neutrophils to fight infection in patients undergoing chemotherapy.[3] Pegfilgrastim has a human half-life of 15 to 80 hours, much longer than the parent filgrastim (3–4 hours).&...

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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/Pegfilgrastim

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Possible Dosages for this and Related Drugs:

Pegfilgrastim-cbqv
  • Injection: 6mg/0.6ml
  • Syringe: 6mg/0.6ml, 6mg/ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Udenyca: (1 result)

Sorted by National Drug Code
  • 70114-101 Udenyca 6 mg/.6ml Subcutaneous Injection, Solution by Coherus Biosciences Inc

Other drugs which contain Pegfilgrastim-cbqv or a similar ingredient: (5 results)




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