The invention discloses an ipiaconitine enteric-coated preparation. The raw materials of the preparation comprise, by weight, 15 to 20 parts of ipiaconitine raw material medicine, 1.5 to 2 parts of dextrin, 1 to 1.5 parts of calcium sulfate, 1.8 to 2 parts of starch, 0.1 to 0.5 part of talcum powder, 2 to 2.5 parts of starch slurry, 4 to 5.3 parts of croscarmellose sodium, 0.5 to 1 part of acrylicresin type I, 0.5 to 1 part of acrylic resin type II, 12 to 15 parts of an ethanol solution, 0.2 to 0.4 part of propylene glycol, 0.3 to 0.5 part of castor oil, 0.1 to 0.5 part of magnesium stearateand 0.03 to 0.05 part of Chinese wax. The ipiaconitine raw material medicine is produced through chemical synthesis and high performance liquid chromatography separation and refining processes. The ipiaconitine enteric-coated preparation is stable in biological activity, simple in pilot plant test process, low in cost, free of disintegration when being eroded by gastric juice, rapid in disintegration when being eroded by intestinal juice, convenient for absorption of effective substances, high in stability, capable of being stored for a long time, common in raw materials and suitable for large-scale production.