Simultaneous Determination and Validation of Hydrochlorothiazide & Eprosartan in bulk drug and Marketed Formulation by Rp-Hplc

Authors

  • Arun Patel Pharmacy department, Shri Ram Group of Institute Faculty of Pharmacy, Jabalpur, 482002, M.P., India.

DOI:

https://doi.org/10.22377/ijpba.v8i1.1514

Abstract

Validation of developed and RP HPLC analytical method according to ICH Guidelines. A review of literature reveals that no analytical methods are available for these drugs. There are no methods in the literature for the estimation of drugs in combined dosage forms. Analytical methods have been report for hydrochlorothiazide and eprosartan using RP-HPLC in pharmaceutical dosage form. The development of simple and precise reverse phase high performance liquid chromatography of hydrochlorothizide and eprosartan using single method in bulk in bulk drug and market formulation.

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Published

2017-05-04

How to Cite

Patel, A. (2017). Simultaneous Determination and Validation of Hydrochlorothiazide & Eprosartan in bulk drug and Marketed Formulation by Rp-Hplc. International Journal of Pharmaceutical & Biological Archive, 8(1). https://doi.org/10.22377/ijpba.v8i1.1514

Issue

Vol. 8 No. 1 (2017): International Journal of Pharmaceutical and Biological Archive

Section

Research Articles

License

This is an Open Access article distributed under the terms of the Attribution-Noncommercial 4.0 International License [CC BY-NC 4.0], which requires that reusers give credit to the creator. It allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, for noncommercial purposes only.