An analytical CE method was developed for the enantiomeric purity determination of fluvastatin enantiomers. Fluvastatin enantiomers were separated on an uncoated fused silica with 100 mM-borate solution containing 30 mg/mL of (2-hydroxypropyl)-$eta$-cyclodextrin (HP-$eta$-CD) as running buffer and fenoprofen as an internal standard. The linearity was observed within a $400-700;{mu}g/mL$ concentration range ($r^2{geq}0.995$) for both fluvastatin enantiomers. The repeatability expressed as coefficient of variation (CV) of the method were 0.96 and 0.92% for (+)-3R, 5S and (-)-3S, 5R-fluvastatin, respectively. The limit of detection and quantification for both fluvastatin enantiomers were $1.5;{mu}g/mL$ and $2.5;{mu}g/mL$, respectively.