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

MR编号	DK/H/0137/005
药品名称	Lornoxicam "Takeda"
活性成分	lornoxicam 8.0 mg
剂型	Powder and solvent for solution for injection
上市许可持有人	Takeda Pharma A/S Delta Park 45, 2665 Vallensbæk Strand, Denmark
参考成员国 - 产品名称	Denmark (DK) Lornoxicam "Nycomed"
互认成员国 - 产品名称
许可日期	2008/04/05
最近更新日期	2024/04/25
药物ATC编码	M01AC Oxicams M01AC05 lornoxicam
申请类型	TypeLevel1：[not specified] TypeLevel2：[not specified] TypeLevel3：[not specified] TypeLevel4：[not specified] TypeLevel5：[not specified]
附件文件下载	Final PL \| Lornoxicam_4mg_common_pl_DK_H123_H137_ cleanDate of last change:2023/07/11 Final Product Information \| Lornoxicam_4mg_common_spc_DK_H123_H137_ cleanDate of last change:2023/07/11 Final SPC \| Lornoxicam_8mg_Inj-common-spc-DK-H123-H137-IIVar_ccds7-cleanDate of last change:2019/10/03 Final SPC \| Lornoxicam_4mg-common-spc-DK-H123-H137-IIVar_ccds7-cleanDate of last change:2019/10/03 Final SPC \| Lornoxicam_8mg-common-spc-DK-H123-H137-IIVar_ccds7-cleanDate of last change:2019/10/03 Final Labelling \| 0137 common-interpack-4mgDate of last change:2018/07/19 Final Labelling \| 0137 common-interpack-8mgDate of last change:2018/07/19 Final Labelling \| 0137 common-interpack-injDate of last change:2018/07/19
市场状态	Positive