药品注册申请号:062373
申请类型:ANDA (仿制药申请)
申请人:BAXTER HLTHCARE
申请人全名:BAXTER HEALTHCARE CORP
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 0.8MG BASE/ML No No None 1982/09/07 1982/09/07 Discontinued
002 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 80MG BASE/100ML No No AP 1982/09/07 Prescription
003 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 40MG BASE/100ML No No None 1982/09/07 Discontinued
004 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 60MG BASE/100ML No No None 1982/09/07 Discontinued
005 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 100MG BASE/100ML No No AP 1982/09/07 Prescription
006 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 120MG BASE/100ML No Yes None 1982/09/07 Prescription
007 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.2MG BASE/ML No No AP 1982/09/07 Prescription
008 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.6MG BASE/ML No No AP 1982/09/07 Prescription
009 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 2MG BASE/ML No Yes None 1982/09/07 Prescription
010 GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 2.4MG BASE/ML No No None 1982/09/07 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
2023/02/10 SUPPL-44(补充) Approval Labeling STANDARD
2023/01/31 SUPPL-42(补充) Approval Labeling STANDARD
2023/01/31 SUPPL-40(补充) Approval Labeling STANDARD
2015/12/11 SUPPL-39(补充) Approval Labeling STANDARD
2013/07/30 SUPPL-35(补充) Approval Labeling
2009/11/30 SUPPL-33(补充) Approval Labeling
2007/11/05 SUPPL-32(补充) Approval Labeling
2004/08/31 SUPPL-31(补充) Approval Labeling
1997/12/29 SUPPL-27(补充) Approval Manufacturing (CMC)
1997/05/21 SUPPL-26(补充) Approval Manufacturing (CMC)
1995/01/27 SUPPL-24(补充) Approval Manufacturing (CMC)
1994/10/17 SUPPL-25(补充) Approval Manufacturing (CMC)
1994/10/17 SUPPL-21(补充) Approval Manufacturing (CMC)
1994/06/28 SUPPL-23(补充) Approval Manufacturing (CMC)
1994/02/25 SUPPL-22(补充) Approval Manufacturing (CMC)
1993/08/04 SUPPL-20(补充) Approval Manufacturing (CMC)
1991/09/10 SUPPL-19(补充) Approval Labeling
1991/06/06 SUPPL-18(补充) Approval Manufacturing (CMC)
1991/03/20 SUPPL-17(补充) Approval Manufacturing (CMC)
1991/02/07 SUPPL-16(补充) Approval Manufacturing (CMC)
1989/05/12 SUPPL-15(补充) Approval Manufacturing (CMC)
1982/09/07 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:GENTAMICIN SULFATE 剂型/给药途径:INJECTABLE;INJECTION 规格:EQ 80MG BASE/100ML 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
062373 002 ANDA GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 80MG BASE/100ML Prescription No No AP 1982/09/07 BAXTER HLTHCARE
062414 008 ANDA GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 80MG BASE/100ML Prescription No No AP 1983/08/15 HOSPIRA
活性成分:GENTAMICIN SULFATE 剂型/给药途径:INJECTABLE;INJECTION 规格:EQ 100MG BASE/100ML 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
062373 005 ANDA GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 100MG BASE/100ML Prescription No No AP 1982/09/07 BAXTER HLTHCARE
062414 010 ANDA GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 100MG BASE/100ML Prescription No No AP 1983/08/15 HOSPIRA
活性成分:GENTAMICIN SULFATE 剂型/给药途径:INJECTABLE;INJECTION 规格:EQ 1.2MG BASE/ML 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
062373 007 ANDA GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.2MG BASE/ML Prescription No No AP 1982/09/07 BAXTER HLTHCARE
062414 001 ANDA GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.2MG BASE/ML Prescription No No AP 1983/08/15 HOSPIRA
活性成分:GENTAMICIN SULFATE 剂型/给药途径:INJECTABLE;INJECTION 规格:EQ 1.6MG BASE/ML 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
062373 008 ANDA GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.6MG BASE/ML Prescription No No AP 1982/09/07 BAXTER HLTHCARE
062414 003 ANDA GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 1.6MG BASE/ML Prescription No No AP 1983/08/15 HOSPIRA
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