批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
>>>原始批准或临时批准<<<
| 审批日期 | 提交号 | 审批结论 | 提交分类 | 审评优先级;罕用药状态 | 通知信、审评文件、说明书、包装标签 | 备注 |
| 2014/05/23 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
PRIORITY
|
|
|
>>>补充申请<<<
| 审批日期 | 提交号 | 审批结论 | 补充类别或审批类型 | 审评优先级;罕用药状态 | 通知信、审评文件、说明书、包装标签 | 备注 |
| 2025/01/13 |
SUPPL-12(补充) |
Approval |
Labeling-Container/Carton Labels,Labeling-Package Insert |
STANDARD
|
|
|
| 2021/07/22 |
SUPPL-10(补充) |
Approval |
Efficacy-New Patient Population |
STANDARD
|
|
|
| 2018/07/24 |
SUPPL-7(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2016/01/20 |
SUPPL-4(补充) |
Approval |
Labeling |
PRIORITY
|
|
|
| 2016/01/20 |
SUPPL-3(补充) |
Approval |
Efficacy-Labeling Change With Clinical Data |
PRIORITY
|
|
Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs. |
| 2015/12/18 |
SUPPL-2(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2014/11/20 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
与本品治疗等效的药品
>>>活性成分:DALBAVANCIN HYDROCHLORIDE; 剂型/给药途径:POWDER;INTRAVENOUS; 规格:EQ 500MG BASE/VIAL; 治疗等效代码:AP<<<
| 申请号 | 产品号 | 申请类型 | 商品名 | 活性成分 | 剂型/给药途径 | 规格 | 市场状态 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
| 218929 |
001 |
ANDA |
DALBAVANCIN HYDROCHLORIDE |
DALBAVANCIN HYDROCHLORIDE |
POWDER;INTRAVENOUS |
EQ 500MG BASE/VIAL |
Prescription |
No |
No |
AP |
--
|
KINDOS |
| 021883 |
001 |
NDA |
DALVANCE |
DALBAVANCIN HYDROCHLORIDE |
POWDER;INTRAVENOUS |
EQ 500MG BASE/VIAL |
Prescription |
Yes |
Yes |
AP |
2014/05/23
|
ABBVIE |
| 219465 |
001 |
ANDA |
DALBAVANCIN HYDROCHLORIDE |
DALBAVANCIN HYDROCHLORIDE |
POWDER;INTRAVENOUS |
EQ 500MG BASE/VIAL |
Prescription |
No |
No |
AP |
2025/10/23
|
TEVA PHARMS INC |
| 217591 |
001 |
ANDA |
DALBAVANCIN HYDROCHLORIDE |
DALBAVANCIN HYDROCHLORIDE |
POWDER;INTRAVENOUS |
EQ 500MG BASE/VIAL |
Prescription |
No |
No |
AP |
2025/11/10
|
FRESENIUS KABI USA |