A Fast, Stability-Indicating, and Validated Liquid Chromatography Method for the Purity Control of Lercanidipine Hydrochloride in Tablet Dosage Form

A robust, sensitive, and stability-indicating rapid resolution liquid chromatography method for the simultaneous determination of process impurities and degradation products of lercanidipine hydrochloride in pharmaceutical dosage form was developed and validated. The chromatographic separation was p...

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Detalles Bibliográficos
Autores principales: Mehta, Saumil, Singh, Sukhdev, Chikhalia, Kishor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065126/
https://www.ncbi.nlm.nih.gov/pubmed/24959405
http://dx.doi.org/10.3797/scipharm.1310-10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065126/
https://www.ncbi.nlm.nih.gov/pubmed/24959405
http://dx.doi.org/10.3797/scipharm.1310-10

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