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Analytical method development and validation of Amlodipine besylate in tablet dosage form
2019
Journal of Drug Delivery and Therapeutics
The accurate and precise HPLC analytical method validated for the determination of Amlodipine besylate in pharmaceutical dosage form.The chromatographic separation is carried out on shimadzu HPLC system (LC-2010 CHT) with UV Vissible detector and C18(150mm x3.9 mm) 5 μm Column. The Mobile phase consists of Acetonitrile: Methanol: PH 3.0 Buffer (15 V: 35 V: 50 V) , at the flow rate of 1.0 ml/min and elutes were monitoring at 237 nm. The observed retention time for Amlodipine besylate was 10.8
doi:10.22270/jddt.v9i4-a.3459
fatcat:cuthrl2cbfduvfg4bka4umchmy