FDA Drug Application (021829) for NEUPRO by UCB INC

Back to FDA Applications sponsored by UCB INC

Application Number021829
Product Number001
FormFILM, EXTENDED RELEASE;TRANSDERMAL
Dosage2MG/24HR
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameNEUPRO
Active IngredientROTIGOTINE



Back to FDA Applications sponsored by UCB INC

Problems, Comments, Suggestions? Click here to contact Greg Thatcher

Please read my Disclaimer





Copyright (c) 2013 Thatcher Development Software, LLC. All rights reserved. No claim to original U.S. Gov't works.