View of Method Development And Validation For The Determination Of Potential Impurities Present In Telmisartan And Hydrochlorothiazide In Fixed Dose Combination Drug Product By Using Reverse Phase - Ultra Performance Liquid Chromatography Coupled With Diode-Array

Return to Article Details Method Development And Validation For The Determination Of Potential Impurities Present In Telmisartan And Hydrochlorothiazide In Fixed Dose Combination Drug Product By Using Reverse Phase - Ultra Performance Liquid Chromatography Coupled With Diode-Array Download Download PDF