药品注册申请号:060733
申请类型:ANDA (仿制药申请)
申请人:PHARMACIA AND UPJOHN
申请人全名:PHARMACIA AND UPJOHN CO
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 BACITRACIN BACITRACIN INJECTABLE;INJECTION 10,000 UNITS/VIAL No No None 1948/07/29 Approved Prior to Jan 1, 1982 Discontinued
002 BACITRACIN BACITRACIN INJECTABLE;INJECTION 50,000 UNITS/VIAL No Yes AP Approved Prior to Jan 1, 1982 Prescription
批准历史,通知信,药品说明书,综述等审批信息
批准日期申请类型申请提交号审查批准结论申请内容分类审评分类(优先审评;罕用药状态)通知信、综述、标签、说明书备注
2004/05/05 SUPPL 12 Approval Labeling
2004/05/05 SUPPL 9 Approval Labeling
2000/04/05 SUPPL 11 Approval Manufacturing (CMC)
1999/12/02 SUPPL 10 Approval Manufacturing (CMC)
1996/09/16 SUPPL 8 Approval Manufacturing (CMC)
1995/03/10 SUPPL 7 Approval Manufacturing (CMC)
1994/04/08 SUPPL 6 Approval Labeling
1991/02/20 SUPPL 5 Approval Manufacturing (CMC)
1948/07/29 ORIG 1 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:BACITRACIN 剂型/给药途径:INJECTABLE;INJECTION 规格:50,000 UNITS/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
060733 002 ANDA BACITRACIN BACITRACIN INJECTABLE;INJECTION 50,000 UNITS/VIAL Prescription No Yes AP Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN
203177 001 ANDA BACITRACIN BACITRACIN INJECTABLE;INJECTION 50,000 UNITS/VIAL Prescription No No AP 2014/08/25 XELLIA PHARMS APS
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药品NDC数据与药品包装、标签说明书
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