药品注册申请号:017858
申请类型:NDA (新药申请)
申请人:SUN PHARM INDS INC
申请人全名:SUN PHARMACEUTICAL INDUSTRIES 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 AN-SULFUR COLLOID TECHNETIUM TC-99M SULFUR COLLOID KIT SOLUTION;INJECTION, ORAL N/A Yes Yes AP 1978/04/17 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
2019/12/19 SUPPL-49(补充) Approval Labeling STANDARD ;Orphan
2016/04/22 SUPPL-40(补充) Approval Manufacturing (CMC) STANDARD
2015/12/04 SUPPL-45(补充) Approval Manufacturing (CMC) STANDARD
2015/09/28 SUPPL-44(补充) Approval Manufacturing (CMC) STANDARD
2015/09/22 SUPPL-43(补充) Approval Manufacturing (CMC) STANDARD
2015/08/13 SUPPL-42(补充) Approval Manufacturing (CMC) STANDARD
2014/09/12 SUPPL-39(补充) Approval Manufacturing (CMC) STANDARD
2013/12/04 SUPPL-38(补充) Approval Manufacturing (CMC) STANDARD
2012/12/14 SUPPL-37(补充) Approval Manufacturing (CMC) STANDARD
2012/08/13 SUPPL-35(补充) Approval Efficacy STANDARD ;Orphan
2011/07/22 SUPPL-34(补充) Approval Efficacy STANDARD
2002/09/13 SUPPL-24(补充) Approval Labeling STANDARD
1998/08/04 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
1995/08/25 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
1989/09/22 SUPPL-20(补充) Approval Labeling
1986/09/12 SUPPL-15(补充) Approval Efficacy
1986/04/02 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1985/08/02 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1985/04/29 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1985/02/26 SUPPL-7(补充) Approval Labeling
1984/09/10 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1982/06/30 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1982/01/27 SUPPL-2(补充) Approval Labeling
1982/01/11 SUPPL-5(补充) Approval Labeling
1981/11/16 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1980/05/11 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1978/04/17 ORIG-1(原始申请) Approval Type 5 - New Formulation or New Manufacturer STANDARD
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
001 ODE 2019/08/13**本条是由Drugfuture回溯的历史信息**
ODE-29 2019/08/13**本条是由Drugfuture回溯的历史信息**
与本品治疗等效的药品
活性成分:TECHNETIUM TC-99M SULFUR COLLOID KIT 剂型/给药途径:SOLUTION;INJECTION, ORAL 规格:N/A 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
017858 001 NDA AN-SULFUR COLLOID TECHNETIUM TC-99M SULFUR COLLOID KIT SOLUTION;INJECTION, ORAL N/A Prescription Yes Yes AP Approved Prior to Jan 1, 1982 SUN PHARM INDS INC
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