药品注册申请号:050709
申请类型:NDA (新药申请)
申请人:ASTELLAS
申请人全名:ASTELLAS PHARMA US 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 PROGRAF TACROLIMUS INJECTABLE;INJECTION EQ 5MG BASE/ML Yes Yes AP 1994/04/08 1994/04/08 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
>>>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
1994/04/08 ORIG-1(原始申请) Approval Type 3 - New Dosage Form PRIORITY ;Orphan
>>>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
2022/11/22 SUPPL-47(补充) Approval Labeling-Package Insert STANDARD
2021/07/16 SUPPL-45(补充) Approval Efficacy-New Indication PRIORITY ;Orphan
2020/12/30 SUPPL-44(补充) Approval Labeling-Package Insert STANDARD
2019/06/11 SUPPL-42(补充) Approval Labeling-Package Insert STANDARD
2018/12/02 SUPPL-41(补充) Approval Labeling-Package Insert STANDARD
2018/05/24 SUPPL-40(补充) Approval Labeling-Package Insert STANDARD
2015/07/01 SUPPL-37(补充) Approval Manufacturing (CMC) PRIORITY
2015/05/19 SUPPL-38(补充) Approval Labeling-Package Insert STANDARD
2013/09/04 SUPPL-36(补充) Approval Labeling-Package Insert STANDARD ;Orphan
2013/08/16 SUPPL-35(补充) Approval Manufacturing (CMC) PRIORITY
2012/08/14 SUPPL-34(补充) Approval Labeling-Package Insert STANDARD
2012/07/05 SUPPL-33(补充) Approval Labeling-Package Insert STANDARD
2012/02/06 SUPPL-31(补充) Approval Labeling-Package Insert STANDARD
2011/07/14 SUPPL-30(补充) Approval Labeling-Package Insert UNKNOWN
2011/07/14 SUPPL-28(补充) Approval Labeling STANDARD
2009/05/19 SUPPL-21(补充) Approval Efficacy-Labeling Change With Clinical Data PRIORITY
2009/02/13 SUPPL-26(补充) Approval Labeling STANDARD
2006/04/27 SUPPL-20(补充) Approval Labeling STANDARD
2006/03/29 SUPPL-19(补充) Approval Efficacy-New Indication STANDARD
2005/12/13 SUPPL-18(补充) Approval Labeling STANDARD
2004/06/16 SUPPL-13(补充) Approval Labeling STANDARD
2001/07/25 SUPPL-12(补充) Approval Labeling STANDARD
2000/12/01 SUPPL-10(补充) Approval Efficacy-Labeling Change With Clinical Data STANDARD
1998/04/20 SUPPL-7(补充) Approval Manufacturing (CMC)-Control PRIORITY
1997/04/22 SUPPL-6(补充) Approval Efficacy-New Indication STANDARD
1997/04/22 SUPPL-5(补充) Approval Efficacy-New Dosing Regimen STANDARD
1996/04/25 SUPPL-4(补充) Approval Labeling STANDARD
1995/06/22 SUPPL-3(补充) Approval Manufacturing (CMC)-Control PRIORITY
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
001 5260301 2011/02/28 Y PDF格式**本条是由Drugfuture回溯的历史信息**
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-294 2025/05/24
ODE-360 2028/07/16
001 ODE 2013/03/29**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:TACROLIMUS; 剂型/给药途径:INJECTABLE;INJECTION; 规格:EQ 5MG 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
050709 001 NDA PROGRAF TACROLIMUS INJECTABLE;INJECTION EQ 5MG BASE/ML Prescription Yes Yes AP 1994/04/08 ASTELLAS
203900 001 ANDA TACROLIMUS TACROLIMUS INJECTABLE;INJECTION EQ 5MG BASE/ML Discontinued No No AP 2017/08/25 HOSPIRA
217108 001 ANDA TACROLIMUS TACROLIMUS INJECTABLE;INJECTION EQ 5MG BASE/ML Prescription No No AP 2025/02/12 NEXUS
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药品NDC数据与药品包装、标签说明书
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