Glyrx-PF

Active Ingredient(s): Glycopyrrolate
FDA Approved: * July 11, 2018
Pharm Company: * EXELA PHARMA SCS LLC
Category: Ulcer

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



Glyrx-PF 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, and inhalated forms. It is a synthetic quaternary amine. 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 approved by ...

Read more Glyrx-PF Details
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 Glyrx-PF: (2 results)

Sorted by National Drug Code
  • 51754-6000 Glyrx-pf .2 mg/ml Intramuscular; Intravenous Injection, Solution by Exela Pharma Sciences, LLC
  • 51754-6001 Glyrx-pf .2 mg/ml Intramuscular; Intravenous Injection, Solution by Exela Pharma Sciences, LLC

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

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