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A new stability-indicating HPLC-UV method was developed for the determination of amlodipine besylate and its impurities, achieving separation within 15 minutes. The method was validated for specificity, accuracy, and robustness, and it effectively resolved degradation products from the amlodipine peak under various stress conditions. This method offers a rapid and environmentally friendly approach for routine quality control of amlodipine besylate in drug substances.
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- officialkiefa10
- Language
- EN