MR编号 | NL/H/3898/003 |
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药品名称 | Rivaroxaban Sandoz 20 mg, filmomhulde tabletten |
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活性成分 | |
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剂型 | Film-coated tablet |
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上市许可持有人 | Sandoz B.V.
Hospitaaldreef 29,
1315 RC Almere
Netherlands |
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参考成员国 - 产品名称 | Netherlands (NL) Rivaroxaban Sandoz 20 mg, filmomhulde tabletten |
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互认成员国 - 产品名称 | - Cyprus (CY)
Rivaroxaban/Sandoz 20mg film-coated tablet - Spain (ES)
- Iceland (IS)
- Germany (DE)
- Denmark (DK)
Rivaroxaban "Sandoz" - Belgium (BE)
Rivaroxaban Sandoz 20 mg filmomhulde tabletten - United Kingdom (Northern Ireland) (XI)
- Ireland (IE)
- Austria (AT)
Rivaroxaban Sandoz 20 mg - Filmtabletten - France (FR)
- Portugal (PT)
- Greece (GR)
RIVAROXABAN/SANDOZ - Sweden (SE)
- Norway (NO)
Rivaroxaban Sandoz - Finland (FI)
- Hungary (HU)
RIVAROXABAN SANDOZ 20 mg filmtabletta - Slovakia (SK)
Rivaroxabán Sandoz 20 mg - Malta (MT)
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许可日期 | 2017/09/01 |
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最近更新日期 | 2024/10/01 |
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药物ATC编码 | |
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申请类型 | - TypeLevel1:Abridged
- TypeLevel2:Additional Strength/Form
- 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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