Development and Validation of a Stability-Indicating RP-HPLC Method for Duloxetine Hydrochloride in its Bulk and Tablet Dosage Form

The objective of the present work was to develop a stability-indicating RP-HPLC method for duloxetine hydrochloride (DUL) in the presence of its degradation products generated from forced decomposition studies. The drug substance was found to be susceptible to stress conditions of acid hydrolysis. T...

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Detalles Bibliográficos
Autores principales: Chhalotiya, Usmangani K., Bhatt, Kashyap K., Shah, Dimal A., Baldania, Sunil L.
Formato: Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2010
Materias:
Original Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007604/
https://www.ncbi.nlm.nih.gov/pubmed/21179321
http://dx.doi.org/10.3797/scipharm.1009-11

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007604/
https://www.ncbi.nlm.nih.gov/pubmed/21179321
http://dx.doi.org/10.3797/scipharm.1009-11

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