“Quantitative Analysis Of Ambroxol Hydrochloride and Bilastine In Bulk and Pharmaceutical Formulations”

M. Pharmacy

The objective of this work was the stability indicating HPLC method for simultaneous estimation of Ambroxol HCL and Bilastine in pharmaceutical formulation. Particular goals were develop a HPLCd for simultaneous estimation of Ambroxol HCl and Bilastine.To validate the method developed using parameters like accuracy, precision, linearity and range for the estimation of these drugs in pharmaceutical dosage form.To obtain the stress degraded products of Ambroxol HCl and Bilastine by exposing a formulation which is under study for different stress conditions like acid, base, oxidative, reductive and neutral media.To study the stress degradation behavior of Ambroxol HCl and Bilastine by analyzing the different products obtained after degradation using HPLC method.To apply the stability indicating HPLC method for the simultaneous estimation of Ambroxol HCL and Bilastine, and degraded product in a pharmaceutical formulation.

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