Abstract
High performance liquid chromatographic method (HPLC) was developed for the Analysis of Levodopa drug was
carried out by 280 nm wave length. This method was found to be linear 25-50 μg/ml of 99% of recoveries. According to
International conference on Harmonization (ICH) guidelines Analytical parameters such as accuracy and precision have
been established for the method for Levodopa tablets and statically to assess the application of the method and It can
be successfully applied for the best analysis of Levedopa drug.
Key Words: Levodopa drug, RP HPLC Method, Propanoic acid, Method validation, Parkinson’s disease