FDA has recently approved a new fixed-dose combination of amlodipine besylate (AMD) and celecoxib (COX) for the treatment\nof hypertension and osteoarthritis. No analytical method has been reported for analysis of these two analytes so far. Hence, to\nmonitor the quality and quantity in the formulation of AMD and COX a simple, accurate, precise, economical, and eco-friendly\nspectroscopic analytical method has been established. The first method involves the determination of AMD and COX by the first\nderivative UV spectroscopic method with scaling factor 10������..
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