Development and Validation of a Stability-Indicating RP-HPLC Method for the Determination of Process-Related Impurities and Degradation Products of Rabeprazole Sodium in Pharmaceutical Formulation

The objective of the current study was to develop and validate a reversed-phase high-performance liquid chromatographic method for the quantitative determination of process-related impurities and degradation products of rabeprazole sodium in pharmaceutical formulation. Chromatographic separation was...

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Detalles Bibliográficos
Autores principales: Kumar, Navneet, Sangeetha, Dhanaraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791934/
https://www.ncbi.nlm.nih.gov/pubmed/24106668
http://dx.doi.org/10.3797/scipharm.1301-25

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791934/
https://www.ncbi.nlm.nih.gov/pubmed/24106668
http://dx.doi.org/10.3797/scipharm.1301-25

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