Novel Validated Stability-Indicating UPLC Method for the Estimation of Naproxen and its Impurities in Bulk Drugs and Pharmaceutical Dosage Form

A novel, reversed-phase ultra-performance liquid chromatographic method was developed and validated for the determination of related substances in Naproxen (NAP) bulk drugs and dosage forms. The related substances included degradation and process-related impurities. The method was developed using th...

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Detalles Bibliográficos
Autores principales: Venkatarao, Papanaboina, Nagendra Kumar, Morrisetty, Ravi Kumar, Maram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528050/
https://www.ncbi.nlm.nih.gov/pubmed/23264943
http://dx.doi.org/10.3797/scipharm.1207-12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3528050/
https://www.ncbi.nlm.nih.gov/pubmed/23264943
http://dx.doi.org/10.3797/scipharm.1207-12

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