药品注册申请号:062588
申请类型:ANDA (仿制药申请)
申请人:HOSPIRA
申请人全名:HOSPIRA 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 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.2MG BASE/ML No No None 1986/01/06 1986/01/06 Discontinued
002 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.4MG BASE/ML No No None 1986/01/06 Discontinued
003 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.6MG BASE/ML No No None 1986/01/06 Discontinued
004 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.8MG BASE/ML No No None 1986/01/06 Discontinued
005 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 2MG BASE/ML No No None 1986/01/06 Discontinued
006 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 60MG BASE/100ML No No None 1986/01/06 Discontinued
007 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 70MG BASE/100ML No No None 1986/01/06 Discontinued
008 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 80MG BASE/100ML No No None 1986/01/06 Discontinued
009 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 90MG BASE/100ML No No None 1986/01/06 Discontinued
010 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 100MG BASE/100ML No No None 1986/01/06 Discontinued
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
1998/12/01 SUPPL-13(补充) Approval Manufacturing (CMC)
1997/06/02 SUPPL-12(补充) Approval Manufacturing (CMC)
1996/07/03 SUPPL-9(补充) Approval Manufacturing (CMC)
1996/03/12 SUPPL-10(补充) Approval Manufacturing (CMC)
1995/08/07 SUPPL-8(补充) Approval Manufacturing (CMC)
1992/03/10 SUPPL-6(补充) Approval Manufacturing (CMC)
1991/04/24 SUPPL-7(补充) Approval Manufacturing (CMC)
1990/08/02 SUPPL-5(补充) Approval Manufacturing (CMC)
1986/01/06 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
本品无治疗等效药品
更多信息
药品NDC数据与药品包装、标签说明书
©2006-2024 DrugFuture->U.S. FDA Drugs Database