药品注册申请号:074686
申请类型:ANDA (仿制药申请)
申请人:TEVA
申请人全名:TEVA 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 GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 1.5MG No No AB 1999/04/20 1999/04/20 Prescription
002 GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 3MG No No AB 1999/04/20 Prescription
003 GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 4.5MG No No None 1999/04/20 Prescription
004 GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 6MG No No AB 1999/04/20 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
2019/10/30 SUPPL-28(补充) Approval Labeling STANDARD
2015/09/02 SUPPL-27(补充) Approval Labeling STANDARD
2014/03/24 SUPPL-25(补充) Approval Labeling STANDARD
2011/08/18 SUPPL-20(补充) Approval Labeling
2010/04/28 SUPPL-19(补充) Approval Labeling
2009/05/06 SUPPL-18(补充) Approval Labeling
2009/05/06 SUPPL-17(补充) Approval Labeling
2002/10/02 SUPPL-10(补充) Approval Manufacturing (CMC)
2002/10/02 SUPPL-9(补充) Approval Manufacturing (CMC)
2002/10/02 SUPPL-8(补充) Approval Manufacturing (CMC)
2002/07/01 SUPPL-7(补充) Approval Manufacturing (CMC)
2000/09/13 SUPPL-6(补充) Approval Manufacturing (CMC)
2000/08/28 SUPPL-4(补充) Approval Manufacturing (CMC)
2000/08/28 SUPPL-3(补充) Approval Labeling
2000/02/15 SUPPL-5(补充) Approval Labeling
1999/04/20 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:GLYBURIDE 剂型/给药途径:TABLET;ORAL 规格:1.5MG 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
020051 001 NDA GLYNASE GLYBURIDE TABLET;ORAL 1.5MG Prescription Yes No AB 1992/03/04 PFIZER
074686 001 ANDA GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 1.5MG Prescription No No AB 1999/04/20 TEVA
075890 001 ANDA GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 1.5MG Discontinued No No AB 2003/07/31 HIKMA
活性成分:GLYBURIDE 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
020051 002 NDA GLYNASE GLYBURIDE TABLET;ORAL 3MG Prescription Yes No AB 1992/03/04 PFIZER
074686 002 ANDA GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 3MG Prescription No No AB 1999/04/20 TEVA
075890 002 ANDA GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 3MG Discontinued No No AB 2003/07/31 HIKMA
活性成分:GLYBURIDE 剂型/给药途径:TABLET;ORAL 规格:6MG 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
020051 004 NDA GLYNASE GLYBURIDE TABLET;ORAL 6MG Prescription Yes Yes AB 1993/09/24 PFIZER
074686 004 ANDA GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 6MG Prescription No No AB 1999/04/20 TEVA
075890 003 ANDA GLYBURIDE (MICRONIZED) GLYBURIDE TABLET;ORAL 6MG Discontinued No No AB 2003/07/31 HIKMA
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