申请人:——
公开号:US20020022649A1
公开(公告)日:2002-02-21
This invention relates to a novel granulate and a novel oral solid dosage formulation, each comprising an active ingredient and one or more carriers prepared by a novel wet granulation method. This method provides that the mixture of active ingredient and carrier be kept below 40° C. during the granulation process such that a more stable formulation is obtained.
本发明涉及一种新型制粒剂和一种新型口服固体制剂,每种制剂都包含一种活性成分和一种或多种载体,采用一种新型湿法制粒法制备。该方法规定,在制粒过程中,活性成分和载体的混合物应保持在 40° C 以下,从而获得更稳定的制剂。