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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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Main Authors: Venkatarao, Papanaboina, Nagendra Kumar, Morrisetty, Ravi Kumar, Maram
Formato: Artigo
Idioma:Inglês
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2012
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3528050/
https://ncbi.nlm.nih.gov/pubmed/23264943
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3797/scipharm.1207-12
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