Two simple, specific, sensitive, accurate and precise stability indicating methods were described forquantitative determinationof theanthelmintics drugNiclosamide. The first method was high performance liquid chromatographic with the use of a reversed phase hibarRC-18 column (250 mm × 4.66 mm, 5 μm) andmobile phaseof methanol: 1mMammonium phosphatebuffer (85:15 v/v) at aflow rateof 1.2mL/min. Theretention timeof drug was found to be 6.45 ± 0.02 min. Quantification of drug was achieved withdiode arraydetection (DAD) at 332nm. Linearcalibration curvewas obtained in concentration range 0.01–100 μg/mL withr2value of 0.999. The limit of detection andlimit of quantificationwere found to be 0.048 μg/mL and 0.01 μg/ml respectively. The second method involved a high performance thin layer liquid chromatographic.Chromatographic separationwas carried out with precoatedsilica gelG60 F254aluminumsheets using toluene:ethyl acetate (7:3% v/v) as amobile phase. Linearity of proposed method was found to be 200–700 ng/band at 332 nm with retention factor of 0.59 andr2value of 0.998. The limit of detection and limit of quantification were found to be 36.21 ng/band and 109.7 ng/band respectively. Both the developed methods were successfully validated as per International Conference on Harmonization guideline (ICH).Niclosamidewas subjected to different stress conditions. The degraded product peaks were well resolved from thepuredrug peak with significant difference in theirretention time. Stress samples were successfully assayed by developed high performance liquid chromatographic and high performance thin layer liquid chromatographic method. Statistically analysis proves that there were no statistical significant differences between two developed methods.