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The document describes the development and validation of a UV spectroscopic method for the simultaneous quantification of atorvastatin and amlodipine in tablet dosage forms. The method utilizes a multi-component mode of analysis and methanol:water as the mobile phase. Validation was performed according to ICH guidelines and showed the method to be linear, accurate, precise and specific for determining atorvastatin and amlodipine concentrations between 70-130% of the test concentration without interference f

Author

sahil

Language

EN