Study on Impurity Profiling of Flavoxate Hydrochloride

The aim of the research project was to test the stability of the drug molecule under a variety of stress conditions as recommended by ICH guidelines and develop a robust analytical HPLC method capable of discriminating between the drug and any possible degradation products.Further the developed method was validated as per the recommendations of ICH guidelines so that the method can be transferred for routine quality control and stability studies of any formulations prepared using Flavoxate Hydrochloride as the active ingredient.