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

MR编号	SK/H/0173/001
药品名称	Paracetamol Dr.Max 500 mg
活性成分	paracetamol 500.0 mg
剂型	Tablet
上市许可持有人	Dr. Max Pharma s.r.o. Na Florenci 2116/15 Nové Město 110 00 Praha 1 Czech republic
参考成员国 - 产品名称	Slovakia (SK) Paracetamol Dr.Max 500 mg
互认成员国 - 产品名称	Italy (IT) Poland (PL) Romania (RO) Czechia (CZ) Paracetamol Saneca 500 mg tablety
许可日期	2017/07/27
最近更新日期	2023/11/17
药物ATC编码	N02BE01 paracetamol
申请类型	TypeLevel1：Known Active Substance TypeLevel2：Initial Application TypeLevel3：Generic Art 10.1 and 10.2 Dir 2001/83/EC TypeLevel4：Chemical Substance TypeLevel5：Non Prescription (including OTC)
附件文件下载	Final Product Information \| common-spc-paracetamol-cleanDate of last change:2021/02/11 Final Product Information \| common-pl-paracetamol-clean_2Date of last change:2021/02/11 Final Product Information \| common-lab-paracetamol-clean_2Date of last change:2021/02/11 Final Labelling \| common-lab-paracetamol-cleanDate of last change:2021/02/11 Final PL \| common-pl-paracetamol-cleanDate of last change:2021/02/11 Final SPC \| common-spc-paracetamol-cleanDate of last change:2021/02/11
市场状态	Positive