This paper describes a sensitive, selective, precise, and stabilityindicating high-performance thin-layer chromatographic method for the determination of fluvoxamine as a bulk drug and in formulation. The method uses aluminium plates precoated with silica gel 60 F-254 as the stationary phase and solvent system ethyl acetatetoluene-methanol-ammonia 7:2:1:0.5 (v/v/v/v). Fluvoxamine was subjected to acid and alkali hydrolysis, oxidation, and photodegradation. The peaks of the degradation products were well resolved from that of the pure drug and had significantly different R F values. The linear regression analysis data for the calibration plots showed a good linear relationship over a concentration range of 100-1000 ng spot -1 . The mean values of the correlation coefficient, slope, and intercept were 0.9992 ± 0.02, 9.8493 ± 0.347, and 386.8 ± 0.71, respectively. Statistical analysis showed that the method is repeatable, selective and can separate the drug from its degradation products and can be used to monitor stability.