A sensitive electroanalytical method for determination of azapropazone  has been  investigated on the basis of the enhancement electrochemical response at glassy carbon electrode during oxidation of azapropazone, Cyclic voltammetric undergo one irreversible anodic peak at Ep = 0.48  mV in Britton - Robinson (BR) (pH 4.0). Cyclic voltammetric study indicated that the oxidation process is irreversible and adsorption controlled. The number of exchanged electrons in the electro -oxidation process was obtained. Differential pulse voltammetry (DPV) and square wave voltammetry (SWV) were studied and a linear calibration obtained from: 0.0014– 0.026µg/ml, 0.014–0.134µg/ml using DPV and SWV respectively. The RSD for five measurements were found in the ranges: 0.854% and 0.911% for DPV and SWV, respectively. Precision and accuracy of the developed method was checked by recovery studies. The method was applied to determine azapropazone in pure form, pharmaceutical formulations, and compared with official methods.