VALIDATED RP HPLC METHOD DEVELOPMENT FOR EXEMESTANE IN TABLET DOSAGE FORM
The aim of this present work was to develop stability indicating LC method, which is selective, accurate, simple, precise, reliable, cost effective and rapid for the quantification of all possible degradants and determination of exemestane. In addition, to develop and validate Stability Indicating Method for the determination of impurities (degradation products) in exemestane API by RP-HPLC. Finally, validate the developed method as per ICH guidelines.
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