欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
HR/H/0264/001
药品名称
Acetylcysteine Sandoz 600 mg
活性成分
Acetylcysteine 600.0 mg
剂型
ORAL POWDER IN SACHET
上市许可持有人
Sandoz B.V. Veluwezoom 22 1327AH Almere Netherlands
参考成员国 - 产品名称
Croatia (HR)
互认成员国 - 产品名称
Austria (AT)
Husten ACC direkt 600 mg - Pulver zum Einnehmen im Beutel
Poland (PL)
ACC Optima Active
Bulgaria (BG)
АЦЦ Инстант 600 mg
Romania (RO)
ACC cu aromă de mure 600 mg pulbere orală în plic
Slovakia (SK)
ACC Long Instant
Slovenia (SI)
许可日期
2017/05/31
最近更新日期
2025/02/05
药物ATC编码
R05CB01 acetylcysteine
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
|
Common PL_cv
Date of last change:2024/09/06
Final SPC
|
Common SPC_cv
Date of last change:2024/09/06
PubAR Summary
|
180108 NL_H_3790_001_DC Acetylcysteine Sandoz summary EN
Date of last change:2024/09/06
PubAR
|
180111 NL_H_3790_001_DC Acetylcysteine Sandoz PAR
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase