欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
CZ/H/0840/003
药品名称
ALTHYXIN
活性成分
Levothyroxine sodium 75.0 µg
剂型
Tablet
上市许可持有人
Zentiva k.s. U kabelovny 130 10237 Praha 10 CZ
参考成员国 - 产品名称
Czechia (CZ)
ALTHYXIN
互认成员国 - 产品名称
Netherlands (NL)
Levothyroxine Abdi 75 microgram tabletten
Poland (PL)
许可日期
2019/11/06
最近更新日期
2024/11/26
药物ATC编码
H03AA01 levothyroxine sodium
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:
Prescription Only
附件文件下载
Final Labelling
|
131_common_interpack_clean
Date of last change:2024/09/06
Final Labelling
|
131_common_outer_clean
Date of last change:2024/09/06
Final SPC
|
131_common_spc_clean
Date of last change:2024/09/06
PubAR
|
CZ_0840_001_8_DC_PAR
Date of last change:2024/09/06
Final PL
|
levothyroxine CZ_H_0840_001_8 name change 16062020 cl
Date of last change:2024/09/06
Final Product Information
|
PI
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase