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This page is a summary of: Development and validation of a stability‐indicating UPLC method for the determination of olmesartan medoxomil, amlodipine and hydrochlorothiazide degradation impurities in their triple‐combination dosage form using factorial design of experiments, Biomedical Chromatography, June 2021, Wiley,
DOI: 10.1002/bmc.5194.
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