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

MR编号	NL/H/0525/001
药品名称	Pravastatine Na CF 10 mg, filmomhulde tabletten
活性成分	pravastatin sodium salt 10.0 mg
剂型	Film-coated tablet
上市许可持有人	Centrafarm B.V. Nieuwe Donk 3 4879 AC ETTEN-LEUR The Netherlands
参考成员国 - 产品名称	Netherlands (NL)
互认成员国 - 产品名称	Luxembourg (LU) Ireland (IE) France (FR) Portugal (PT) Denmark (DK) Austria (AT) Pravastatin "Stada" 10 mg-Filmtabletten
许可日期	2004/09/09
最近更新日期	2024/03/12
药物ATC编码	C10AA03 pravastatin
申请类型	TypeLevel1：Abridged TypeLevel2：Multiple (Copy) Application TypeLevel3：Generic Article 4.8(a)(iii), first paragraph TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	Final PL \| 1_3_1_PIL_common_en_NL_H_0525_001_003_clDate of last change:2024/03/12 Final SPC \| 1_3_1_SPC_common_en_NL_H_0525_001_003_clDate of last change:2024/03/12 Final Labelling \| common-spc pravastatine Na CFDate of last change:2018/12/04 Final Labelling \| common-outer pack pravastatine Na CF 10 mgDate of last change:2018/12/04 Final Labelling \| common-pl pravastatine NA CFDate of last change:2018/12/04 Final Labelling \| common-outer pack pravastatine Na CF 20 mgDate of last change:2018/12/04 Final Labelling \| common-outer pack pravastatine Na CF 40 mgDate of last change:2018/12/04
市场状态	Positive