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Journal of Pharmaceutical and Biomedical Analysis

Volumn 39, Issue 3-4, 2005, Pages 517-522

Development and validation of a reversed-phase HPLC method for the determination of ezetimibe in pharmaceutical dosage forms

(5) Sistla, R a Tata, V S S K a Kashyap, Y V a Chandrasekar, D a Diwan, P V a

a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY (India)

Author keywords

Ezetimibe; Hypercholesterolemia; Reversed phase HPLC; Tablets

Indexed keywords

EZETIMIBE;

ANALYTIC METHOD; ANALYTICAL EQUIPMENT; ARTICLE; DRUG DETERMINATION; ELUTION; PRIORITY JOURNAL; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; TABLET; VALIDATION PROCESS;

ACETONITRILES; ANTICHOLESTEREMIC AGENTS; AZETIDINES; CALIBRATION; CHEMISTRY, PHARMACEUTICAL; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG INDUSTRY; DRUG STABILITY; ENTEROCYTES; HEPTANES; HYDROGEN-ION CONCENTRATION; HYPERCHOLESTEROLEMIA; MODELS, CHEMICAL; PHARMACEUTICAL PREPARATIONS; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; SPECTROPHOTOMETRY, ULTRAVIOLET; SULFONIC ACIDS; TABLETS; TEMPERATURE; TIME FACTORS; ULTRAVIOLET RAYS;

EID: 23944443039 PISSN: 07317085 EISSN: None Source Type: Journal
DOI: 10.1016/j.jpba.2005.04.026 Document Type: Article

Times cited : (164)

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