Analytical methods development and validation play important roles in the discovery, development, and manufacture of pharmaceuticals. Recent days, HPLC (High performance liquid chromatography) is the method of choice used by the pharmaceutical industry to assay the intact drug and degradation products. The present text book concentrated on method development and validation of simultaneous estimation levofloxacin and azithromycin in tablet formulations. It explains step by step procedure for the development and validation of a RP-HPLC method for a selected combination of drugs. This book is useful guide for the simultaneous estimation of levofloxacin and azithromycin for routine analysis of tablet formulations in Industry and academic research.
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