Development and validation of a dissolution test with reversed-phase high performance liquid chromatographic analysis for Candesartan cilexetil in tablet dosage forms
Development and validation of a dissolution test with reversed-phase high performance liquid chromatographic analysis for Candesartan cilexetil in tablet dosage forms
Authors
Keywords
In vitro, release, Candesartan cilexetil, Validation, Reversed-phase high performance liquid chromatography
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