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Drug profile · INN

rotigotine

NEUPRO

FDA: approved EMA: approved TGA: approved NMPA: clinical trials N04BC09
US status
approved
Patents linked
0
News articles
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Quick answer

rotigotine (NEUPRO) is an FDA-listed pharmaceutical active ingredient. Route of administration: transdermal. Current US regulatory status: approved.

Key facts

INN rotigotine
Brand NEUPRO
Route TRANSDERMAL
Formulation FILM, EXTENDED RELEASE
ATC code N04BC09

Frequently asked questions

What is rotigotine?

rotigotine (NEUPRO) is an FDA-listed pharmaceutical active ingredient. Route of administration: transdermal. Current US regulatory status: approved.

What is the brand name for rotigotine?

NEUPRO is a marketed brand name for rotigotine. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of rotigotine?

rotigotine has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.