Fast dissolving tablets are designed to dissolve or disintegrate rapidly in the saliva generally in less than 60 seconds. Prepared tablets were evaluated for their physicochemical properties. Powder blend were evaluated for various parameters like angle of repose, bulk density, tapped density, compressibility index, Hausner’s ratio. Directly compressed tablets were analyzed for the uniformity of drug content, thickness, hardness, weight variation, friability and in-vitro dissolution study. F6 formulation showed maximum drug release of 99.087%. The release of F8, F7, F4 was 95.986%, 97.484%, 93.867% respectively and for marketed preparation, it was 80.497%. The stability studies of the optimized formulation F6 tablets revealed that there was no significant change in the physical parameters when stored at temperature and humidity conditions of 45±2°C/75±5 % RH and at room temperature.
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