药品注册申请号:050742
申请类型:NDA (新药申请)
申请人:MERCK SHARP DOHME
申请人全名:MERCK SHARP AND DOHME 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001 STROMECTOL IVERMECTIN TABLET;ORAL 6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1996/11/22 1996/11/22 Discontinued
002 STROMECTOL IVERMECTIN TABLET;ORAL 3MG Yes Yes AB 1998/10/08 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
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
2022/03/14 SUPPL-30(补充) Approval Labeling STANDARD
2015/05/11 SUPPL-28(补充) Approval Manufacturing (CMC)
2015/04/07 SUPPL-27(补充) Approval Manufacturing (CMC)
2009/12/15 SUPPL-26(补充) Approval Labeling STANDARD
2009/06/11 SUPPL-25(补充) Approval Labeling STANDARD
2009/06/11 SUPPL-24(补充) Approval Labeling STANDARD
2009/05/01 SUPPL-23(补充) Approval Labeling STANDARD
2008/09/12 SUPPL-22(补充) Approval Labeling STANDARD
2008/02/26 SUPPL-20(补充) Approval Manufacturing (CMC)
2007/09/26 SUPPL-21(补充) Approval Labeling STANDARD
2007/09/26 SUPPL-19(补充) Approval Labeling STANDARD
2006/01/20 SUPPL-18(补充) Approval Labeling STANDARD
2006/01/20 SUPPL-17(补充) Approval Labeling STANDARD
2004/11/18 SUPPL-15(补充) Approval Labeling STANDARD
2004/02/12 SUPPL-13(补充) Approval Labeling STANDARD
2004/02/12 SUPPL-12(补充) Approval Labeling STANDARD
2003/01/15 SUPPL-11(补充) Approval Labeling STANDARD
2002/12/12 SUPPL-8(补充) Approval Manufacturing (CMC)
2002/05/28 SUPPL-7(补充) Approval Manufacturing (CMC)
2001/07/17 SUPPL-6(补充) Approval Manufacturing (CMC)
2001/01/04 SUPPL-5(补充) Approval Labeling STANDARD
2001/01/04 SUPPL-2(补充) Approval Labeling STANDARD
1999/11/10 SUPPL-4(补充) Approval Manufacturing (CMC)
1999/08/04 SUPPL-3(补充) Approval Manufacturing (CMC)
1998/10/08 SUPPL-1(补充) Approval Manufacturing (CMC)
1996/11/22 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity 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
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:IVERMECTIN 剂型/给药途径:TABLET;ORAL 规格:3MG 治疗等效代码:AB
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
050742 002 NDA STROMECTOL IVERMECTIN TABLET;ORAL 3MG Prescription Yes Yes AB 1998/10/08 MERCK SHARP DOHME
204154 001 ANDA IVERMECTIN IVERMECTIN TABLET;ORAL 3MG Prescription No No AB 2014/10/24 EDENBRIDGE PHARMS
218324 001 ANDA IVERMECTIN IVERMECTIN TABLET;ORAL 3MG Prescription No No AB 2024/10/16 SENORES PHARMS
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