The prime objective for carrying out present study was to develop analytical Profile for drug and simultaneous quantitation of drug and its process related impurities. This has been achieved successfully.RP-HPLC methods were developed for simultaneous quantitative estimation of impurity and drug. Validation of developed method was carried out successfully. On the basis of results and statistical evaluation like coefficient of correlation, RSD it can be said that the developed method is simple, precise, accurate, rapid and economic for quantitation of impurity and drug.