欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
NL/H/3256/005
药品名称
Levobupivacaine Molteni 7,5 mg/ml
活性成分
levobupivacaine hydrochloride 7.5 mg/ml
剂型
Solution for injection/infusion
上市许可持有人
L. Molteni & C. dei F.lli Alitti Societa di Es. S.p.A. Strada Statale 67, Fraz. Granatieri, 50018 Scandicci, Firenze, Italy
参考成员国 - 产品名称
Netherlands (NL)
Levobupivacaïne Molteni 7,5 mg/ml, oplossing voor injectie/infusie
互认成员国 - 产品名称
Italy (IT)
许可日期
2015/05/13
最近更新日期
2022/12/15
药物ATC编码
N01BB10 levobupivacaine
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
附件文件下载
PubAR Summary
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160429 NL_H_3256_001_005_DC Levobupivacaine Molteni summary EN
Date of last change:2024/09/06
PubAR
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160706 NL_H_3256_001_005_DC Levobupivacaine Molteni PAR
Date of last change:2024/09/06
Final SPC
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final _ clean SmPC _ Ampoules
Date of last change:2024/09/06
Final Labelling
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final _ clean Labelling interpack _ Bags
Date of last change:2024/09/06
Final Labelling
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final _ clean Inner labelling _ Ampoules
Date of last change:2024/09/06
Final Labelling
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final _ clean Outer labelling _ Ampoules
Date of last change:2024/09/06
Final Labelling
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final _ clean Outer labelling _ Bags
Date of last change:2024/09/06
Final PL
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final _ clean PL _ Ampoules
Date of last change:2024/09/06
Final Labelling
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final clean _ Labelling impack_ Bags
Date of last change:2024/09/06
Final PL
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final clean _ PL _ Bags
Date of last change:2024/09/06
Final SPC
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NL_H_3256_001_005_DC _ Levobupivacaine Molteni _ final clean _ SmPC _ Bags
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase