Neupro

Active Ingredient(s): Rotigotine
FDA Approved: * May 9, 2007
Pharm Company: * SCHWARZ
Category: Parkinsons

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



Neupro Overview

Rotigotine, sold under the brand name Neupro among others, is a dopamine agonist of the non-ergoline class of medications indicated for the treatment of Parkinson's disease (PD) and restless legs syndrome (RLS).[1][2] It is formulated as a once-daily transdermal patch which provides a slow and constant supply of the drug over the course of 24 hours.[1] Like other dopamine agonists, rotigotine has been shown to possess antidepressant effects and ...

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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/Rotigotine

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Possible Dosages for this and Related Drugs:

Rotigotine
  • Film, Extended Release: 1mg/24hr, 2mg/24hr, 3mg/24hr, 4mg/24hr, 6mg/24hr, 8mg/24hr
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Neupro: (7 results)

Sorted by National Drug Code
  • 50474-801 Neupro 1 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-802 Neupro 2 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-803 Neupro 3 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-804 Neupro 4 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-805 Neupro 6 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-806 Neupro 8 mg/24h Transdermal Patch, Extended Release by Ucb, Inc.
  • 50474-808 Neupro Kit by Ucb, Inc.

Other drugs which contain Rotigotine or a similar ingredient: (1 result)