QbD based development of HPLC method for simultaneous quantification of Telmisartan and Hydrochlorothiazide impurities in tablets dosage form

A simple reverse phase liquid chromatographic gradient method has been developed and validated for the simultaneous determination of specified & un-specified impurities of Telmisartan and Hydrochlorothiazide in combination oral solid dosage forms. The developed method is effective to separate a...

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Veröffentlicht in:	Practical laboratory medicine Jg. 21; S. e00169
Hauptverfasser:	Palakurthi, Ashok K., Dongala, Thirupathi, Katakam, Lakshmi Narasimha R.
Format:	Journal Article
Sprache:	Englisch
Veröffentlicht:	Elsevier B.V 01.08.2020 Elsevier
Schlagworte:	Analytical quality by design Design of experiments HPLC-UV Hydrochlorothiazide Solid dosage form Stability indicating Telmisartan Solid dosage form Stability indicating Analytical quality by design Hydrochlorothiazide Design of experiments HPLC-UV Telmisartan
ISSN:	2352-5517, 2352-5517
Online-Zugang:	Volltext
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