Stability-Indicating RP-HPLC Method Development and Validation for Duloxetine Hydrochloride in Tablets

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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. The drug was found to be stable to dry heat, photodegradation, oxidation and basic condition attem...

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ژورنال

عنوان ژورنال: Journal of AOAC INTERNATIONAL

سال: 2010

ISSN: 1060-3271,1944-7922

DOI: 10.1093/jaoac/93.1.123