Xuriden

Active Ingredient(s): Uridine Triacetate
FDA Approved: * September 4, 2015
Pharm Company: * WELLSTAT THERAPEUTICS CORP
Category: Genetic Disorders

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



Xuriden Overview

Uridine is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, a ribofuranose) via a β-N1-glycosidic bond. It is one of the five standard nucleosides which make up nucleic acids, the others being adenosine, thymidine, cytidine and guanosine. The five nucleosides are commonly abbreviated to their one-letter codes U, A, T, C and G respectively. However, thymidine is more commonly written as 'dT' ('d' represents 'deoxy') as it contains a 2'-de...

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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/Uridine

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Possible Dosages for this and Related Drugs:

Uridine Triacetate
  • Granule: 0.1g, 10gm/packet, 120mg/kg, 2gm/packet, 60mg/kg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Xuriden: (1 result)

Sorted by National Drug Code
  • 69468-152 Xuriden 951 mg/g Oral Granule by Wellstat Therapeutics Corporation

Other drugs which contain Uridine Triacetate or a similar ingredient: (2 results)






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