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
>>>原始批准或临时批准<<<
| 审批日期 | 提交号 | 审批结论 | 提交分类 | 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 |
| 1982/09/07 |
ORIG-1(原始申请) |
Approval |
|
|
|
|
>>>补充申请<<<
| 审批日期 | 提交号 | 审批结论 | 补充类别或审批类型 | 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-Package Insert |
STANDARD
|
|
|
| 2023/01/31 |
SUPPL-42(补充) |
Approval |
Labeling-Container/Carton Labels |
STANDARD
|
|
|
| 2023/01/31 |
SUPPL-40(补充) |
Approval |
Labeling-Container/Carton Labels,Labeling-Package Insert |
STANDARD
|
|
|
| 2015/12/11 |
SUPPL-39(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2013/07/30 |
SUPPL-35(补充) |
Approval |
Labeling-Package Insert |
|
|
|
| 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) |
|
|
|
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 |
| 无 |
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 | RLD | RS | TE 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 |
Discontinued |
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 | RLD | RS | TE 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 |
Discontinued |
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 | RLD | RS | TE 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 |
Discontinued |
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 | RLD | RS | TE 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 |
Discontinued |
No |
No |
AP |
1983/08/15
|
HOSPIRA |