FDA Drug Application (200834) for VENLAFAXINE HYDROCHLORIDE by AUROBINDO PHARMA LTD

Back to FDA Applications sponsored by AUROBINDO PHARMA LTD

Application Number200834
Product Number001
FormCAPSULE, EXTENDED RELEASE;ORAL
DosageEQ 37.5MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameVENLAFAXINE HYDROCHLORIDE
Active IngredientVENLAFAXINE HYDROCHLORIDE



Back to FDA Applications sponsored by AUROBINDO PHARMA LTD

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.