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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Hlavní autoři: Mehta, Saumil, Singh, Sukhdev, Chikhalia, Kishor
Médium: Artigo
Jazyk:Inglês
Vydáno: Österreichische Apotheker-Verlagsgesellschaft 2014
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4065126/
https://ncbi.nlm.nih.gov/pubmed/24959405
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3797/scipharm.1310-10
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