A validated stability-indicating liquid chromatographic method for determination of process related impurities and degradation behavior of Irbesartan in solid oral dosage

The present work describes the development and validation of a stability-indicating RP-HPLC method for the estimation of degradation and process related impurities of Irbesartan, namely Impurity-1, Impurity-2, Impurity-3 and Impurity-4. The developed LC method was validated with respect to specifici...

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Detalles Bibliográficos
Autor principal: Goswami, Nishant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960792/
https://www.ncbi.nlm.nih.gov/pubmed/24695518
http://dx.doi.org/10.4103/2231-4040.126985

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960792/
https://www.ncbi.nlm.nih.gov/pubmed/24695518
http://dx.doi.org/10.4103/2231-4040.126985

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