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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...

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Bibliografiske detaljer
Main Authors: Trivedi, Rakshit Kanubhai, Patel, Mukesh C.
Format: Artigo
Sprog:Inglês
Udgivet: Österreichische Apotheker-Verlagsgesellschaft 2011
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3097508/
https://ncbi.nlm.nih.gov/pubmed/21617775
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3797/scipharm.1009-12
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