In the present study parameters for validation of analytical method spectrophotometric to quantifying Mebendazole Suspension was carried. We performed an analysis of Mebendazole 100 mg/5ml Suspension, lot 00202027 (Instituto Quimioterápico S.A. - IQFARMA). Formic acid were used as solvents and isopropyl alcohol. The method used in this report proved to be selective in determining the analyte between the excipients, the samples were subjected to degradation by UV getting 99,932% for the sample and radiated 100,016% for non-irradiated sample. The test Linearity introduced a correlation coefficient of 0.9998; Test Statistical Linearity and Response Factor, expressed conformity. For the study of Accuracy, the percentage of recovery was 100736. In Test G Cochran was lower than G Experimental Tables (0,4315 <0,8709). For statistical Student t test was smaller than t Experimental Table (1,861 ...

They determined the parameters for the revalidation of the analytical method spectrophometric to 310 nm (TPT126 review 05), proposed by the Institute laboratory Quimioterápico SA (IQFARMA) for the quantification of Mebendazole tablets. We performed an analysis of Mebendazole 100 mg tablets lot 00101007. Formic acid and alcohol isopropílico were used like solvents. Getting in the trial of Linearity a correlation coefficient of 0.9999; Test Statistical Linearity and Response Factor, expressed conformity. For accuracy, the percentage of recovery was 100,885. In the Test G Cochran was obtained G Exp. Tables G minor (0.4993 <0.8709). For statistical Student's t test was obtained t Exp. Less than t Table (2,169 <2,306), the accuracy is correct according to their respective specifications. In assessing accuracy, repeatability of the test showed a concentration averaged 101,344 mg per tablet w...