药品注册申请号:062251
申请类型:ANDA (仿制药申请)
申请人:HIKMA
申请人全名:HIKMA PHARMACEUTICALS USA 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 GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 40MG BASE/ML No No AP 1980/06/05 Approved Prior to Jan 1, 1982 Prescription
002 GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 10MG BASE/ML No No AP Approved Prior to Jan 1, 1982 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
2022/02/15 SUPPL-30(补充) Approval Labeling STANDARD
2001/07/23 SUPPL-28(补充) Approval Manufacturing (CMC)
2001/07/23 SUPPL-27(补充) Approval Manufacturing (CMC)
2001/07/23 SUPPL-26(补充) Approval Manufacturing (CMC)
1999/10/14 SUPPL-25(补充) Approval Manufacturing (CMC)
1999/02/11 SUPPL-24(补充) Approval Manufacturing (CMC)
1994/02/03 SUPPL-21(补充) Approval Manufacturing (CMC)
1993/09/16 SUPPL-20(补充) Approval Manufacturing (CMC)
1991/11/18 SUPPL-19(补充) Approval Manufacturing (CMC)
1991/05/31 SUPPL-17(补充) Approval Manufacturing (CMC)
1991/05/17 SUPPL-18(补充) Approval Manufacturing (CMC)
1991/02/08 SUPPL-16(补充) Approval Manufacturing (CMC)
1990/11/19 SUPPL-15(补充) Approval Manufacturing (CMC)
1988/07/12 SUPPL-14(补充) Approval Manufacturing (CMC)
1988/02/22 SUPPL-13(补充) Approval Manufacturing (CMC)
1987/05/22 SUPPL-11(补充) Approval Manufacturing (CMC)
1980/06/05 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 40MG 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
062251 001 ANDA GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 40MG BASE/ML Prescription No No AP Approved Prior to Jan 1, 1982 HIKMA
062366 001 ANDA GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 40MG BASE/ML Prescription No Yes AP 1983/08/04 FRESENIUS KABI USA
062420 002 ANDA GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 40MG BASE/ML Prescription No No AP 1983/08/15 HOSPIRA
215237 001 ANDA GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 40MG BASE/ML Prescription No No AP 2024/01/08 EUGIA PHARMA
活性成分:GENTAMICIN SULFATE 剂型/给药途径:INJECTABLE;INJECTION 规格:EQ 10MG 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
062251 002 ANDA GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 10MG BASE/ML Prescription No No AP Approved Prior to Jan 1, 1982 HIKMA
062420 001 ANDA GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 10MG BASE/ML Prescription No No AP 1983/08/15 HOSPIRA
062366 002 ANDA GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 10MG BASE/ML Prescription No Yes AP 1986/02/06 FRESENIUS KABI USA
215236 001 ANDA GENTAMICIN SULFATE GENTAMICIN SULFATE INJECTABLE;INJECTION EQ 10MG BASE/ML Prescription No No AP 2024/01/08 EUGIA PHARMA
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