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 (trade name Neupro) 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][1] Like other dopamine agonists, rotigotine has been shown to possess antidepressant effects and may be us...

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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)

ROTIGOTINE