The present invention provides a process for preparing high purity cilostazol.

Provided is a cilostazol preparation which comprises incorporating a fine powder of cilostazol into a dispersing and/or solubilizing agent thereby to enhance the dispersibility and/or solubility.

Cilostazol improves your ability to walk longer distances without pain.

Medication to improve walking distance, such as cilostazol (Pletal)

This result is similar with Vedavathi et al. [12] , Prakash et al. [13] and Umamaheswar et al. [14] .

A process for the preparation of compounds of formula (III), intermediates useful for the synthesis of cilostazol, which process comprises reacting haloimine of formula (V) wherein X is halogen, with trimethylsilyl azide.

Cilostazol are used to treat intermittent claudication.

Such is the case with the councils (sagti or sagyan) in the Theravda.

Cilostazol (Pletal), may improve the distance you are able to walk without pain.

The present invention relates to the new use of Cilostazol, ie, the use of it in preparing the medicine for bradycardia treatment.

Due to the cyclodextrin, the solubility of the cilostazol or salt in the water is heightened.

Cilostazol is used to treat the symptoms of intermittent claudication.

Cilostazol and several of its metabolites are inhibitors of phosphodiesterase III.

Cilostazol and many of its metabolites inhibit phosphodiesterase III.

Cilostazol is used to treat intermittent claudication.