The present invention relates to a suspension comprising non-micronized ezetimibe micro-particles having small particle size and high specific surface area wherein said ezetimibe micro-particles are prepared without micronization process, and wherein the process prevents secondary agglomeration of the ezetimibe micro-particles in the suspension. The suspension of non-micronized ezetimibe micro-particles can be directly used in the process of the preparation of pharmaceutical composition. The present invention relates to non-micronized ezetimibe micro-particles having small particle size and high specific surface area that can be recovered from the suspension.