FDA Drug Application (084773) for PREDNISOLONE by AUROLIFE PHARMA LLC

Back to FDA Applications sponsored by AUROLIFE PHARMA LLC

Application Number084773
Product Number001
FormTABLET;ORAL
Dosage5MG
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NamePREDNISOLONE
Active IngredientPREDNISOLONE



Back to FDA Applications sponsored by AUROLIFE PHARMA LLC

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.