Utibron Neohaler

Active Ingredient(s): Indacaterol + Glycopyrrolate
FDA Approved: * October 29, 2015
Pharm Company: * NOVARTIS PHARMS CORP
Category: Lungs (Pulmonary)

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



Utibron Neohaler Overview

Indacaterol (INN) is an ultra-long-acting beta-adrenoceptor agonist[1] developed by Novartis. It was approved by the European Medicines Agency (EMA) under the trade name Onbrez Breezhaler on November 30, 2009,[2] and by the United States Food and Drug Administration (FDA), under the trade name Arcapta Neohaler, on July 1, 2011.[3] It needs to be taken only once a day,[4] unlike the related drugs formoterol and salmeterol. It is l...

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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/Indacaterol

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Possible Dosages for this and Related Drugs:

Indacaterol + Glycopyrrolate
  • Powder: 15.6mcg/inh + 27.5mcg/inh, 27.5mcg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Utibron Neohaler: (2 results)

Sorted by National Drug Code
  • 0078-0664 Utibron Neohaler Respiratory (Inhalation) Capsule by Novartis Pharmaceuticals Corporation
  • 63402-681 Utibron Neohaler Respiratory (Inhalation) Capsule by Sunovion Pharmaceuticals Inc.

Drugs with one or more similar ingredients: (12 results)




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