Abstract

Rapid and sensitive UV Spectrophotometric approach for regular assessment of hypertensive medication. For the assessment of drugs in their formulation, a brand-new, secure, and sensitive method of spectrophotometric estimate in the UV-region has been created. The analysis’s complete set of parameters were selected in accordance with ICH guidelines and statistically confirmed. System suitability, specificity, precision linearity, accuracy, intraday and interday assays, robustness, ruggedness, LOD, and log experiments were done. There was no excipient or other additive interference while calculating the Commercial Formulation.