| MR编号 | NL/H/4213/001 |
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| 药品名称 | Emtricitabine/Tenofovirdisoproxil Accordpharma |
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| 活性成分 | - emtricitabine 200.0 mg
- TENOFOVIR DISOPROXIL FUMARATE 300.0 mg
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| 剂型 | Film-coated tablet |
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| 上市许可持有人 | Accord Healthcare B.V.
Winthontlaan 200
3526 KV Utrecht
The Netherlands |
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| 参考成员国 - 产品名称 | Netherlands (NL) Emtricitabine/Tenofovir disoproxil Accordpharma 200 mg/245 mg filmomhulde tabletten RVG 122434 |
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| 互认成员国 - 产品名称 | - Denmark (DK)
- Iceland (IS)
Emtricitabine/Tenofovir disoproxil Accordpharma 200 mg/245 mg filmuhúðuð tafla - United Kingdom (Northern Ireland) (XI)
- Ireland (IE)
- Austria (AT)
Emtricitabin/Tenofovirdisoproxil Accordpharma 200 mg/245 mg Filmtabletten - Spain (ES)
- Sweden (SE)
- Norway (NO)
Emtricitabine/Tenofovir disoproxil Accordpharma - Finland (FI)
- Latvia (LV)
Emtricitabine/Tenofovir disoproxil Accordpharma 200 mg/245 mg apvalkotās tabletes - Lithuania (LT)
Emtricitabine/Tenofovir disoproxil Accordpharma 200 mg/245 mg plėvele dengtos tabletės - Estonia (EE)
EMTRICITABINE/TENOFOVIR DISOPROXIL ACCORDPHARMA - Hungary (HU)
EMTRICITABINE/TENOFOVIR DISOPROXIL ACCORDPHARMA 200 mg/245 mg filmtabletta - Slovenia (SI)
Emtricitabin/dizoproksiltenofovirat Accordpharma 200 mg/245 mg filmsko obložene tablete
|
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| 许可日期 | 2019/04/03 |
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| 最近更新日期 | 2024/09/03 |
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| 药物ATC编码 | - J05AR03 tenofovir disoproxil and emtricitabine
|
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| 申请类型 | - TypeLevel1：Known Active Substance
- 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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