Cuvposa

Active Ingredient(s): Glycopyrrolate
FDA Approved: * July 28, 2010
Pharm Company: * SHIONOGI PHARMA
Category: Ulcer

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



Cuvposa Overview

Glycopyrronium bromide is a medication of the muscarinic anticholinergic group. It does not cross the blood–brain barrier and consequently has no to few central effects. It is available in by mouth, intravenous, topical, and inhalated forms. It is a synthetic quaternary ammonium . It was developed by Sosei and licensed to Novartis in 2005. The cation, which is the active moiety, is called glycopyrronium (INN)[1] or glycopyrrolate (USAN). In June 2018, glycopyrronium was...

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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/Glycopyrrolate

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Possible Dosages for this and Related Drugs:

Glycopyrrolate
  • Injection: 0.2mg/ml
  • Powder: 15.6mcg, 15.6mcg/inh
  • Solution: 0.2mg/ml, 0.2mg/ml (0.2mg/ml), 0.4mg/2ml (0.2mg/ml), 1mg/5ml, 25mcg/ml
  • Tablet: 1.5mg, 1mg, 2mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Cuvposa: (2 results)

Sorted by National Drug Code
  • 0259-0501 Cuvposa 1 mg/5ml Oral Liquid by Merz Pharmaceuticals, LLC
  • 59630-206 Cuvposa 1 mg/5ml Oral Solution by Shionogi Pharma, Inc.

Other drugs which contain Glycopyrrolate or a similar ingredient: (10 results)






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