MR编号 | NL/H/5834/001 |
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药品名称 | Pomalidomide Sandoz 1 mg, hard capsules |
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活性成分 | |
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剂型 | Capsule, hard |
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上市许可持有人 | Sandoz B.V.
Veluwezoom 22
1327 AH Almere
The Netherlands |
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参考成员国 - 产品名称 | Netherlands (NL) Pomalidomide Sandoz 1 mg, harde capsules |
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互认成员国 - 产品名称 | - Denmark (DK)
Pomalidomide "Sandoz" - Latvia (LV)
- Iceland (IS)
- Lithuania (LT)
Pomalidomide Sandoz 1 mg kietosios kapsulės - Ireland (IE)
- Estonia (EE)
- Austria (AT)
- Hungary (HU)
Pomalidomide Sandoz - France (FR)
- Cyprus (CY)
Pomalidomide/Sandoz 1mg hard capsules - Spain (ES)
- Czechia (CZ)
Pomalidomid Sandoz - Italy (IT)
- Romania (RO)
- Greece (GR)
- Slovakia (SK)
- Sweden (SE)
- Slovenia (SI)
- Norway (NO)
- Malta (MT)
- Finland (FI)
- Germany (DE)
Pomalidomid HEXAL 1 mg Hartkapseln - Poland (PL)
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许可日期 | 2024/06/07 |
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最近更新日期 | 2025/01/29 |
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药物ATC编码 | |
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申请类型 | - TypeLevel1:Abridged
- TypeLevel2:Initial Application
- TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
- TypeLevel4:Chemical Substance
- TypeLevel5:Prescription Only
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附件文件下载 | |
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市场状态 | Positive |
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