LIQUID-CHROMATOGRAPHIC ANALYSIS OF RANITIDINE HYDROCHLORIDE IN PHARMACEUTICAL PREPARATIONS

被引：2
|
作者：
ENEIN, HYA
ISLAM, MR
机构：
[1] Drug Development Laborator), Radionuclide and Cyclotron Operations Department, King Faisal Specialist Hospital and Research Centre, Riyadh 11211
来源：
TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY | 1990年 / 29卷 / 01期
关键词：
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY (HPLC); DETERMINATION; RANITIDINE; PHARMACEUTICAL PREPARATIONS;
D O I：
10.1080/02772249009357616
中图分类号：
X [环境科学、安全科学];
学科分类号：
08 ; 0830 ;
摘要：
A sensitive, accurate and reproducible method for the analysis of ranitidine in pharmaceutical preparations has been described. An isocratic HPLC elution method was employed which requires about 10 minutes to be performed. The concentration of ranitidine hydrochloride preparations was found to be 98.19 ±0.02% and 98.33 ±0.04% in Zantac® and Apo-ranitidine® tablets, respectively. © 1990, Taylor & Francis Group, LLC. All rights reserved.
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页码：47 / 51
页数：5
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