Validation of the method for determination of related impurities in the active antiviral ingredient of enisamium iodide

The aim of the work. To validate a method for the related impurities determination in the enisamium iodide active pharmaceutical ingredient (API) by means of high-performance liquid chromatography (HPLC). To characterize the sensitivity of the method by establishing the limit of detection and limit...

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Bibliographic Details
Main Authors: O. V. Burmaka, S. M. Hureieva, V. M. Marhitych
Format: Article
Language:English
Published: Zaporozhye State Medical University 2018-10-01
Series:Zaporožskij Medicinskij Žurnal
Subjects:
Online Access:http://zmj.zsmu.edu.ua/article/view/141718/141121