欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	DE/H/4682/003
药品名称	Sitaplis 100 mg Filmtabletten
活性成分	SITAGLIPTIN malate 132.88 mg
剂型	Film-coated tablet
上市许可持有人	HWI pharma services GmbH Rheinzaberner Straße 8 D-76761 Rülzheim Germany
参考成员国 - 产品名称	Germany (DE) SITAPLIS 100 mg Filmtabletten
互认成员国 - 产品名称	Luxembourg (LU) Sitaplis, 100 mg, Comprimé pelliculé
许可日期	2017/02/28
最近更新日期	2019/03/06
药物ATC编码	A10BH01 sitagliptin
申请类型	TypeLevel1：Abridged TypeLevel2：Additional Strength/Form TypeLevel3：Generic Art 10.1 and 10.2 Dir 2001/83/EC TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	PAR \| DE4681_4682_01-03_DC'_Sitaclar_Sitagliptin_final PARDate of last change:2018/09/19 Final Product Information \| common-final-spc-4681-4682(001)-V001Date of last change:2017/12/21 Final Product Information \| common-final-pl-4681-4682(001)-V001Date of last change:2017/12/21 Final Product Information \| common-final-pl-4681-4682(002)-V001Date of last change:2017/12/21 Final Product Information \| common-final-pl-4681-4682(003)-V001Date of last change:2017/12/21 Final Product Information \| common-final-spc-4681-4682(002)-V001Date of last change:2017/12/21 Final Product Information \| common-final-spc-4681-4682(003)-V001Date of last change:2017/12/21
市场状态	Positive