药品注册申请号:021337
申请类型:NDA (新药申请)
申请人:MSD SUB MERCK
申请人全名:MERCK SHARP AND DOHME LLC A SUB OF MERCK AND CO INC
产品信息
产品号商品名活性成分剂型/给药途径规格/剂量参比药物(RLD)生物等效参考标准(RS)治疗等效代码该申请号批准日期该产品号批准日期市场状态
001 INVANZ ERTAPENEM SODIUM INJECTABLE;INTRAMUSCULAR, INTRAVENOUS EQ 1GM BASE/VIAL Yes Yes AP 2001/11/21 2001/11/21 Prescription
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
提交状态日期提交号审批结论申请内容分类审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
2022/03/17 SUPPL-51(补充) Approval Labeling STANDARD
2020/12/22 SUPPL-49(补充) Approval Labeling STANDARD
2019/09/20 SUPPL-48(补充) Approval Labeling STANDARD
2018/12/19 SUPPL-47(补充) Approval Labeling STANDARD
2018/09/12 SUPPL-46(补充) Approval Labeling STANDARD
2017/09/08 SUPPL-45(补充) Approval Labeling STANDARD Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs.
2015/03/16 SUPPL-43(补充) Approval Manufacturing (CMC) STANDARD
2014/09/30 SUPPL-42(补充) Approval Labeling STANDARD
2013/08/05 SUPPL-40(补充) Approval Manufacturing (CMC) STANDARD
2013/07/24 SUPPL-41(补充) Approval Labeling STANDARD
2013/01/18 SUPPL-39(补充) Approval Manufacturing (CMC) STANDARD
2012/03/02 SUPPL-38(补充) Approval Labeling STANDARD
2012/02/17 SUPPL-37(补充) Approval Labeling STANDARD
2011/07/22 SUPPL-31(补充) Approval Labeling STANDARD
2010/05/25 SUPPL-34(补充) Approval Labeling UNKNOWN
2009/12/13 SUPPL-30(补充) Approval Labeling STANDARD
2009/10/06 SUPPL-33(补充) Approval Labeling UNKNOWN
2008/03/25 SUPPL-28(补充) Approval Labeling STANDARD
2007/11/16 SUPPL-26(补充) Approval Labeling STANDARD
2006/12/28 SUPPL-25(补充) Approval Manufacturing (CMC) N/A
2006/08/10 SUPPL-21(补充) Approval Efficacy STANDARD
2005/10/14 SUPPL-19(补充) Approval Efficacy STANDARD
2005/05/18 SUPPL-18(补充) Approval Efficacy PRIORITY
2005/01/24 SUPPL-17(补充) Approval Labeling STANDARD
2004/09/10 SUPPL-15(补充) Approval Labeling STANDARD
2004/05/20 SUPPL-14(补充) Approval Labeling STANDARD
2004/04/30 SUPPL-13(补充) Approval Labeling STANDARD
2002/12/20 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
2002/07/09 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
2002/05/09 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
2002/05/09 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
2001/11/21 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity STANDARD
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号专利号专利过期日是否物质专利是否产品专利专利用途代码撤销请求提交日期专利下载备注
001 5478820 2015/11/21 Y Y U-160 PDF格式**本条是由Drugfuture回溯的历史信息**
5478820*PED 2016/05/21 PDF格式**本条是由Drugfuture回溯的历史信息**
5652233 2013/02/02 Y Y U-160 PDF格式**本条是由Drugfuture回溯的历史信息**
5652233*PED 2013/08/02 PDF格式**本条是由Drugfuture回溯的历史信息**
5952323 2017/05/15 Y PDF格式**本条是由Drugfuture回溯的历史信息**
5952323*PED 2017/11/15 PDF格式**本条是由Drugfuture回溯的历史信息**
7342005 2013/02/02 Y PDF格式**本条是由Drugfuture回溯的历史信息**
7342005*PED 2013/08/02 PDF格式**本条是由Drugfuture回溯的历史信息**
与本品相关的市场独占权保护信息
关联产品号独占权代码失效日期备注
001 I-476 2008/10/14**本条是由Drugfuture回溯的历史信息**
I-515 2009/08/10**本条是由Drugfuture回溯的历史信息**
NCE 2006/11/21**本条是由Drugfuture回溯的历史信息**
NPP 2008/05/18**本条是由Drugfuture回溯的历史信息**
PED 2007/05/21**本条是由Drugfuture回溯的历史信息**
PED 2008/11/18**本条是由Drugfuture回溯的历史信息**
与本品治疗等效的药品
活性成分:ERTAPENEM SODIUM 剂型/给药途径:INJECTABLE;INTRAMUSCULAR, INTRAVENOUS 规格:EQ 1GM 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RLDRSTE Code产品号批准日期申请人
021337 001 NDA INVANZ ERTAPENEM SODIUM INJECTABLE;INTRAMUSCULAR, INTRAVENOUS EQ 1GM BASE/VIAL Prescription Yes Yes AP 2001/11/21 MSD SUB MERCK
208790 001 ANDA ERTAPENEM SODIUM ERTAPENEM SODIUM INJECTABLE;INTRAMUSCULAR, INTRAVENOUS EQ 1GM BASE/VIAL Prescription No No AP 2018/04/16 ACS DOBFAR SPA
209133 001 ANDA ERTAPENEM SODIUM ERTAPENEM SODIUM INJECTABLE;INTRAMUSCULAR, INTRAVENOUS EQ 1GM BASE/VIAL Prescription No No AP 2018/06/25 EUGIA PHARMA
207647 001 ANDA ERTAPENEM SODIUM ERTAPENEM SODIUM INJECTABLE;INTRAMUSCULAR, INTRAVENOUS EQ 1GM BASE/VIAL Prescription No No AP 2019/03/19 SAVIOR LIFETEC CORP
212040 001 ANDA ERTAPENEM SODIUM ERTAPENEM SODIUM INJECTABLE;INTRAMUSCULAR, INTRAVENOUS EQ 1GM BASE/VIAL Prescription No No AP 2021/03/26 GLAND PHARMA LTD
209145 001 ANDA ERTAPENEM SODIUM ERTAPENEM SODIUM INJECTABLE;INTRAMUSCULAR, INTRAVENOUS EQ 1GM BASE/VIAL Discontinued No No AP 2023/05/02 SUN PHARM
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