Rayaldee

Active Ingredient(s): Calcifediol
FDA Approved: * June 17, 2016
Pharm Company: * OPKO IRELAND GLOBAL HOLDINGS LTD
Category: Osteoporosis

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



Rayaldee Overview

Calcifediol, also known as calcidiol, 25-hydroxycholecalciferol, or 25-hydroxyvitamin D (abbreviated 25(OH)D),[1] is a prehormone that is produced in the liver by hydroxylation of vitamin D3 (cholecalciferol) by the enzyme cholecalciferol 25-hydroxylase. Physicians worldwide measure this metabolite to determine a patient's vitamin D status.[2][3] At a typical daily intake of vitamin D3, its full conversion to calcifediol takes approximately 7 da...

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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/Calcifediol

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Possible Dosages for this and Related Drugs:

Calcifediol
  • Capsule: 0.02mg, 0.05mg, 20mcg
  • Capsule, Extended Release: 0.03mg, 30mcg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Rayaldee: (1 result)

Sorted by National Drug Code
  • 70301-1001 Rayaldee 30 ug/1 Oral Capsule, Extended Release by Opko Pharmaceuticals LLC

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




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