Development of validated stability-indicating chromatographic method for the determination of fexofenadine hydrochloride and its related impurities in pharmaceutical tablets
Open Access
- 3 December 2011
- journal article
- Published by Springer Science and Business Media LLC in Chemistry Central Journal
- Vol. 5 (1), 76
- https://doi.org/10.1186/1752-153x-5-76
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Simultaneous determination of phthalates and adipates in human serum using gas chromatography–mass spectrometry with solid‐phase extractionBiomedical Chromatography, 2010
- Rapid RP-LC Method with Fluorescence Detection for Analysis of Fexofenadine in Human PlasmaChromatographia, 2010
- Measurement of fexofenadine concentration in micro‐sample human plasma by a rapid and sensitive LC‐MS/MS employing protein precipitation: application to a clinical pharmacokinetic studyBiomedical Chromatography, 2009
- Validated LC Method, with a Chiral Mobile Phase, for Separation of the Isomers of Fexofenadine HydrochlorideChromatographia, 2008
- Isolation and structure elucidation of photodegradation products of fexofenadineJournal of Pharmaceutical and Biomedical Analysis, 2008
- Development and validation of a rapid RP-HPLC method for the determination of cetirizine or fexofenadine with pseudoephedrine in binary pharmaceutical dosage formsJournal of Pharmaceutical and Biomedical Analysis, 2008
- Determination of Fexofenadine in Tablets by Capillary Electrophoresis in Free Solution and in Solution with Cyclodextrins as Analyte CarriersDrug Development and Industrial Pharmacy, 2005
- Efficacy and safety profile of fexofenadine HCL: A unique therapeutic option in H1-receptor antagonist treatmentJournal of Allergy and Clinical Immunology, 2003
- The choice of an H1 -antihistamine for the 21st centuryClinical & Experimental Allergy Reviews, 2002
- Practical HPLC method development : Wiley, New York, 1988 (ISBN 0-471-62782-8). xvi + 260 pp. Price £35.00Analytica Chimica Acta, 1991