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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Vydané v:	Practical laboratory medicine Ročník 21; s. e00169
Hlavní autori:	Palakurthi, Ashok K., Dongala, Thirupathi, Katakam, Lakshmi Narasimha R.
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	Elsevier B.V 01.08.2020 Elsevier
Predmet:	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
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