欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0399/002
药品名称
Moxonur 0,3 mg
活性成分
moxonidine 0.3 mg
剂型
Film-coated tablet
上市许可持有人
Ratiopharm GmbH Graf-Arco-Str.3, D-89079 Ulm, Germany
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Germany (DE)
许可日期
2003/08/05
最近更新日期
2024/07/01
药物ATC编码
C02AC05 moxonidine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial 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
|
Moxonidine-OuterPack-20.02.13
Date of last change:2013/04/27
Final Product Information
|
Moxonidine-SPC-20.02.13
Date of last change:2013/04/27
Final Product Information
|
Moxonidine-PIL 20.02.13
Date of last change:2013/04/27
Final SPC
|
common-spc-clean
Date of last change:2012/07/12
Final PL
|
common-pl-clean
Date of last change:2012/07/12
市场状态
Positive
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