FDA Drug Application (076607) for QUINAPRIL HYDROCHLORIDE by SUN PHARM INDS LTD

Back to FDA Applications sponsored by SUN PHARM INDS LTD

Application Number076607
Product Number001
FormTABLET;ORAL
DosageEQ 5MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameQUINAPRIL HYDROCHLORIDE
Active IngredientQUINAPRIL HYDROCHLORIDE



Back to FDA Applications sponsored by SUN PHARM INDS 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.