A Review on Development and validation of analytical method for estimation of Rifapentine in bulk and Pharmaceutical formulation

A simple analytical Method is developed for identification and quantification of related impurities in the API and pharmaceutical dosage form. Rifapentine is an antibiotic from the rifamycin class that is utilized in the treatment of tuberculosis. The solvent, method, analytical procedure, reaction time, Solvent concentration used are carefully optimized with Maximum sensitivity. The developed method is Validated as per the guidelines of International Conference Harmonization (ICH.) the proposed method is precise and accurate and for the routine analysis of Rifapentine hence can be used for bulk and pharmaceutical dosage form.