The present research work discusses the development of a stability-indicating UV spectrophotometric method for the estimation of Ofloxacin and Flavoxate hydrochloride in tablet dosage form. The optimum conditions for the analysis of the drug were established. The maximum wavelength (λmax) was found to be 266 nm for ofloxacin and 272 nm for flavoxate. Degradation studies of ofloxacin and flavoxate showed prominent degradation in acid hydrolysis.
Keywords
Stability Indicating, Ofloxacin, Flavoxate, UV Spectrophotometry.
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