FDA Drug Application (017543) for LUDIOMIL by NOVARTIS

Back to FDA Applications sponsored by NOVARTIS

Application Number017543
Product Number001
FormTABLET;ORAL
Dosage25MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameLUDIOMIL
Active IngredientMAPROTILINE HYDROCHLORIDE



Back to FDA Applications sponsored by NOVARTIS

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.