Development and Validation of a Stability Indicating RP-UPLC Method for Determination of Quetiapine in Pharmaceutical Dosage Form

The present work reports a stability indicating reversed phase ultra performance liquid chromatography (RP-UPLC) method for the quantitative determination of quetiapine in pharmaceutical dosage form. The chromatographic separation is performed on an Agilent Eclipse Plus C18, RRHD 1.8 μm (50 mm x 2.1...

Descripción completa

Detalles Bibliográficos
Autores principales: Trivedi, Rakshit Kanubhai, Patel, Mukesh C.
Formato: Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3097508/
https://www.ncbi.nlm.nih.gov/pubmed/21617775
http://dx.doi.org/10.3797/scipharm.1009-12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3097508/
https://www.ncbi.nlm.nih.gov/pubmed/21617775
http://dx.doi.org/10.3797/scipharm.1009-12

Ejemplares similares