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

American Journal of PharmTech Research

, R. Murali Krishna¹  R. Srikanth Reddy² 

[1] 2.PNCO Department, Andhra University, Visakhapatnam - 530 003,Andhra Pradesh,;1.APL Research centre (A division of Aurobindo Pharma Limited), Survey No. 313, Bachupally, Quthubullapur Mandal, Ranga reddy District, Hyderabad, Telangana-500090, India.

关键词: Telmisartan;    Hydrochlorothiazide;    Forced Degradation;    RP-UPLC and Stability Indicating;   

DOI  :  10.21276/ajptr

学科分类：药学

来源: American Journal Of Pharmtech Research

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