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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Detalles Bibliográficos
Autores principales: Palakurthi, Ashok K., Dongala, Thirupathi, Katakam, Lakshmi Narasimha R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322094/
https://www.ncbi.nlm.nih.gov/pubmed/32613068
http://dx.doi.org/10.1016/j.plabm.2020.e00169

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322094/
https://www.ncbi.nlm.nih.gov/pubmed/32613068
http://dx.doi.org/10.1016/j.plabm.2020.e00169

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