Indian J Pharm Sci. Nov;72(6) doi: /X RP - HPLC method for the estimation of Tamsulosin Hydrochloride in Tablet Dosage Form. Kumari R(1), Dash PP, Lal VK, Mishra A, Murthy PN. Author information: (1)Sagar Institute of Technology and Management, Barabanki - , India. stability indicating method for the determination of tamsulosin in presence of its degradation products and for assessment of purity of bulk drug and stability of its dosage forms. Stability. RP-HPLC Method for the Determination of Tamsulosin in Bulk and. Pharmaceutical Dosage Forms. T.K. LAHA, S. MISHRA and S. SEN.
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A rapid and sensitive reverse phase RP-HPLC method is proposed for the estimation of tamsulosin hydrochloride in tablets. Tamsulosin hydrochloride was chromatographed on a reverse phase C18 column with a mobile phase consisting of acetonitrile and water in the ratio of v/v. The mobile phase was pumped at a. Stability-Indicating RP-HPLC Method for Determination of. Tamsulosin HCL in Pharmaceutical Dosage Form. G S Kumar* and B Sai Pavan Kumar. Department of Pharmaceutical Analysis & Quality Assurance, GITAM Institute of Pharmacy, GITAM University, Visakhapatnam - , India. INTRODUCTION: Tamsulosin HCl.
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A simple, rapid, precise and flushed isocratic reversed-phase HPLC method was approved and validated for the intramuscular determination of Dutasteride (DTA) and Tamsulosin (TMS) in divided tablets. The tamsulosin hplc analysis has helped adequate separation for DTA and TMS from your associated tamsulosin hplc analyses of the tablets. A petted stability-indicating reversed phase high-performance liquid chromatographic mist method was developed and wondered for quantitative determination of tamsulosine hydrochloride in reducing drugs and in pharmaceutical dosage guide in the transition of degradation products. An isocratic, emerging phase HPLC ins.
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