欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/3711/001
药品名称
L-Thyroxin-Na AbZ 88 Mikrogramm Tabletten
活性成分
Levothyroxine sodium 0.09 mg
剂型
Tablet
上市许可持有人
AbZ-Pharma GmbH Graf-Arco-Str. 3 DE-89079 Ulm Germany
参考成员国 - 产品名称
Germany (DE)
L-Thyroxin-Na AbZ 88 Mikrogramm, Tabletten
互认成员国 - 产品名称
许可日期
2013/12/13
最近更新日期
2024/12/17
药物ATC编码
H03AA01 levothyroxine sodium
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Other Generic application Art 10.3 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final SPC
|
levothyroxine_de_h_3711_001_002_smpc_28_05_24
Date of last change:2024/12/17
Final PL
|
levothyroxine_de_h_3711_001_002_pil_28_05_24
Date of last change:2024/12/17
PubAR
|
04_DE_3687_3710_3711_001_003_DC_L_thyroxine_final PAR
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label immediate blisters Levothyroxine Sodium 0_088mg_clean
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label immediate blisters Levothyroxine Sodium 0_112mg_clean
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label immediate blisters Levothyroxine Sodium 0_137mg_clean
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label_outer Levothyroxine Sodium Teva 0_088mg
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label_outer Levothyroxine Sodium Teva 0_088mg_clean
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label_outer Levothyroxine Sodium Teva 0_112mg
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label_outer Levothyroxine Sodium Teva 0_112mg_clean
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label_outer Levothyroxine Sodium Teva 0_137mg
Date of last change:2024/09/06
Final Labelling
|
1_3_1 label_outer Levothyroxine Sodium Teva 0_137mg_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase