| MR编号 | NL/H/4508/004 |
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| 药品名称 | Dailiport 3 mg |
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| 活性成分 | - Tacrolimus monohydrate 3.0 mg
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| 剂型 | Prolonged-release capsule, hard |
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| 上市许可持有人 | Sandoz B.V.
Hospitaaldreef 29
1315 RC Almere
Nederland |
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| 参考成员国 - 产品名称 | Netherlands (NL) Dailiport 3 mg, harde capsules met verlengde afgifte RVG 123568 |
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| 互认成员国 - 产品名称 | - Norway (NO)
- Denmark (DK)
Dailiport - Belgium (BE)
Dailiport 3 mg capsules met verlengde afgifte - Iceland (IS)
Dailiport forðahylki - United Kingdom (Northern Ireland) (XI)
- Austria (AT)
Dailiport 3 mg - Hartkapseln, retardiert - Portugal (PT)
- Sweden (SE)
- Finland (FI)
- Poland (PL)
Dailiport - Latvia (LV)
Dailiport 3 mg ilgstošās darbības cietās kapsulas - Lithuania (LT)
Dailiport 3 mg pailginto atpalaidavimo kietosios kapsulės - Estonia (EE)
DAILIPORT - Czechia (CZ)
Dailiport - Slovakia (SK)
Dailiport 3 mg - Slovenia (SI)
Dailiport 3 mg trde kapsule s podaljšanim sproščanjem - Germany (DE)
Dailiport 3 mg Hartkapseln, retardiert
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| 许可日期 | 2019/09/18 |
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| 最近更新日期 | 2025/02/03 |
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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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