The invention relates to an oral delivery vehicle tablet formed by compression of a plurality of particles, wherein the oral delivery vehicle tablet comprises a sugar alcohol in an amount of 40-99.9% by weight of the delivery vehicle tablet, wherein the oral delivery vehicle tablet comprises: A combination comprising non-directly compressible (non-DC) erythritol particles in an amount of 15-50% by weight of the delivery vehicle tablet, wherein the oral delivery vehicle tablet is granulated into a sugar alcohol in an amount of 0.1-6% by weight of the tablet. The one or more binders other than the agent, wherein the delivery vehicle tablet comprises a plurality of further sugar alcohol particles in an amount of at least 10% by weight of the delivery vehicle tablet, and wherein the further sugar alcohol particles comprise the non- It relates to an oral delivery vehicle tablet having a different composition than DC erythritol.本発明は、複数の粒子の圧縮によって形成される経口送達ビヒクル錠剤であって、経口送達ビヒクル錠剤が、送達ビヒクル錠剤の40～99.9質量%の量で糖アルコールを含み、経口送達ビヒクル錠剤が、送達ビヒクル錠剤の15～50質量%の量で非直接圧縮性(非DC)エリスリトール粒子を含み、経口送達ビヒクル錠剤が、錠剤の0.1～6質量%の量で、糖アルコールに造粒される結合剤以外の1つ又は複数の結合剤を含み、送達ビヒクル錠剤が、送達ビヒクル錠剤の少なくとも10質量%の量で複数の更なる糖アルコール粒子を含み、及び前記更なる糖アルコール粒子が、前記非DCエリスリトールとは異なる組成物を有する、経口送達ビヒクル錠剤に関する。
