欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0408/002
药品名称
Moxonidine 0,3 mg
活性成分
moxonidine 0.0 [no unit]
剂型
Film-coated tablet
上市许可持有人
Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Belgium (BE)
United Kingdom (Northern Ireland) (XI)
许可日期
2003/08/05
最近更新日期
2022/10/20
药物ATC编码
C02AC05 moxonidine
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 Product Information
|
common-pl-0-3mg
Date of last change:2020/07/13
Final Product Information
|
common-outer
Date of last change:2020/07/13
Final Product Information
|
common-pl-0-2mg
Date of last change:2020/07/13
Final Product Information
|
common-pl-0-4mg
Date of last change:2020/07/13
Final Product Information
|
common-spc
Date of last change:2020/07/13
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase