The ongoing way of multiplication in Codiaeum aucobifolium L. is cutting of the leafy stems, which is not completely successful and it could increase the number of infected plants. To proliferation plant tissue technique was used. The explants of leaves and internodes were cultured on 2, 4-D (1 mg/lit) supplemented media including: (Mitra & chaturvedi, Anderson, Murashige & Skoog). The An medium was the best in regard to the production of big and fresh calli. In the other experiment was studied only in An by adding different concentrations of BAP (0, 0.5, 1, 2, and 4 mg/lit) Together various dilutions of one of the auxins including: IAA, 2, 4-D or NAA. Callus induction was greatest in IAA (4 mg/lit)+BAP (1 mg/lit), NAA (2 mg/lit)+BAP (1 mg/lit) and 2, 4-D (1 mg/lit) alone. To evaluate the organogenesis, the greenest cultured Calli were Subcultured in the media supplemented by various concentrations of different cytokinins (2ip, BAP, Kin, and coconut milk) and above auxins. The most excellent organogenesis was achived in coconut milk (20%)+2, 4-D (1 mg/lit). The best combinations for elongation and proliferation of shoots were 2ip (1 mg/lit) + IAA (0.5 mg/lit) and IAA (2 mg/lit) + BAP (1 mg/lit) respectively.