药品注册申请号:062640
申请类型:ANDA (仿制药申请)
申请人:ACS DOBFAR
申请人全名:ACS DOBFAR SPA
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 CEFTAZIDIME CEFTAZIDIME INJECTABLE;INJECTION 500MG/VIAL No No None 1985/11/20 1985/11/20 Discontinued
002 CEFTAZIDIME CEFTAZIDIME INJECTABLE;INJECTION 1GM/VIAL No Yes AP 1985/11/20 Prescription
003 CEFTAZIDIME CEFTAZIDIME INJECTABLE;INJECTION 2GM/VIAL No Yes AP 1985/11/20 Prescription
004 CEFTAZIDIME CEFTAZIDIME INJECTABLE;INJECTION 6GM/VIAL No Yes AP 1992/02/03 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
2021/07/16 SUPPL-45(补充) Approval Labeling STANDARD
2021/07/16 SUPPL-44(补充) Approval Labeling STANDARD
2020/02/13 SUPPL-42(补充) Approval Labeling STANDARD
2020/02/13 SUPPL-40(补充) Approval Labeling STANDARD
2013/02/11 SUPPL-34(补充) Approval Labeling
2012/03/16 SUPPL-33(补充) Approval Labeling
2009/04/07 SUPPL-30(补充) Approval Labeling
2006/09/08 SUPPL-24(补充) Approval Labeling
1996/08/15 SUPPL-20(补充) Approval Manufacturing (CMC)
1996/07/15 SUPPL-21(补充) Approval Labeling
1996/02/26 SUPPL-19(补充) Approval Labeling
1993/10/18 SUPPL-18(补充) Approval Manufacturing (CMC)
1992/02/14 SUPPL-14(补充) Approval Labeling
1992/02/14 SUPPL-13(补充) Approval Labeling
1992/02/14 SUPPL-10(补充) Approval Labeling
1992/02/03 SUPPL-15(补充) Approval Labeling
1988/08/26 SUPPL-9(补充) Approval Manufacturing (CMC)
1988/08/04 SUPPL-8(补充) Approval Manufacturing (CMC)
1985/11/20 ORIG-1(原始申请) Approval
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
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
与本品治疗等效的药品
活性成分:CEFTAZIDIME 剂型/给药途径:INJECTABLE;INJECTION 规格:1GM/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
050578 002 NDA FORTAZ CEFTAZIDIME INJECTABLE;INJECTION 1GM/VIAL Discontinued Yes No AP 1985/07/19 PAI HOLDINGS PHARM
062640 002 ANDA CEFTAZIDIME CEFTAZIDIME INJECTABLE;INJECTION 1GM/VIAL Prescription No Yes AP 1985/11/20 ACS DOBFAR
062662 002 ANDA TAZICEF CEFTAZIDIME INJECTABLE;INJECTION 1GM/VIAL Prescription No No AP 1986/03/06 HOSPIRA
064032 001 ANDA TAZICEF CEFTAZIDIME INJECTABLE;INJECTION 1GM/VIAL Prescription No No AP 1993/10/31 HOSPIRA
活性成分:CEFTAZIDIME 剂型/给药途径:INJECTABLE;INJECTION 规格:2GM/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
050578 003 NDA FORTAZ CEFTAZIDIME INJECTABLE;INJECTION 2GM/VIAL Discontinued Yes No AP 1985/07/19 PAI HOLDINGS PHARM
062640 003 ANDA CEFTAZIDIME CEFTAZIDIME INJECTABLE;INJECTION 2GM/VIAL Prescription No Yes AP 1985/11/20 ACS DOBFAR
062662 003 ANDA TAZICEF CEFTAZIDIME INJECTABLE;INJECTION 2GM/VIAL Prescription No No AP 1986/03/06 HOSPIRA
064032 002 ANDA TAZICEF CEFTAZIDIME INJECTABLE;INJECTION 2GM/VIAL Prescription No No AP 1993/10/31 HOSPIRA
活性成分:CEFTAZIDIME 剂型/给药途径:INJECTABLE;INJECTION 规格:6GM/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
050578 004 NDA FORTAZ CEFTAZIDIME INJECTABLE;INJECTION 6GM/VIAL Discontinued Yes No AP 1985/07/19 PAI HOLDINGS PHARM
062662 004 ANDA TAZICEF CEFTAZIDIME INJECTABLE;INJECTION 6GM/VIAL Prescription No No AP 1986/03/06 HOSPIRA
062640 004 ANDA CEFTAZIDIME CEFTAZIDIME INJECTABLE;INJECTION 6GM/VIAL Prescription No Yes AP 1992/02/03 ACS DOBFAR
更多信息
药品NDC数据与药品包装、标签说明书
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