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The proposed methods were validated. The accuracy of the methods was assessed by recovery studies at three different levels. Recovery experiments indicated the absence of interference from commonly encountered pharmaceutical additives. The method was found to be precise as indicated by the repeatability analysis, showing %RSD less than 2. All statistical data proves validity of the methods and can be used for routine analysis of pharmaceutical dosage form. It can be effectively applied for routine analysis in research institutions, quality control department in meant in industries, approved testing laboratories studies in near future.


Atomoxetine, repeatability analysis, high resolution, retention time

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