Nocdurna

Active Ingredient(s): Desmopressin Acetate
FDA Approved: * June 21, 2018
Pharm Company: * FERRING PHARMS INC
Category: Diabetes

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



Nocdurna Overview

Desmopressin, sold under the trade name DDAVP among others, is a medication used to treat diabetes insipidus, bedwetting, hemophilia A, von Willebrand disease, and high blood urea levels.[1] In hemophilia A and von Willebrand disease, it should only be used for mild to moderate cases.[1] It may be given in the nose, by injection into a vein, by mouth, or under the tongue.[1] Common side effects include headaches, diarrhea, and low blood sodium.[1] The low blood sodium that results may cause s...

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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/Desmopressin

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Possible Dosages for this and Related Drugs:

Desmopressin Acetate
  • Injection: 0.004mg/ml, 0.015mg/ml, 4mcg/ml
  • Solution: 0.01%
  • Spray: 0.83mcg/0.1ml, 1.66mcg/0.1ml
  • Spray, Metered: 0.00083mg/spray, 0.00166mg/spray, 0.01mg/actuation, 0.01mg/spray, 0.15mg/spray, 1.5mg/spray, 150mcg/actuation
  • Tablet: 0.1mg, 0.2mg, 27.7mcg, 53.3mcg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Nocdurna: (2 results)

Sorted by National Drug Code
  • 55566-5050 Nocdurna 27.7 ug/1 Sublingual Tablet by Ferring Pharmaceuticals Inc.
  • 55566-5070 Nocdurna 55.3 ug/1 Sublingual Tablet by Ferring Pharmaceuticals Inc.

Other drugs which contain Desmopressin Acetate or a similar ingredient: (7 results)





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