| 摘要 |
<p>An orally administered tablet comprising a therapeutic amount of a pharmaceutically acceptable salt of amiodarone (e.g., an acid salt of amiodarone such as amiodarone hydrochloride) is described. Other ingredients include a disaccharide which is preferably a reducing disaccharide, pregelatinized starch, and an alkali metal starch glycolate. The tablet preferably also comprises at least one of the following: a) 2 to 6 % by weight stearic acid, b) less than 1 % by weight magnesium stearate, c) 2 to 25 % by weight of wet binder, and d) less than 0.1 % by weight of silica gel.</p> |
