药品注册申请号:050592
申请类型:NDA (新药申请)
申请人:SANDOZ
申请人全名:SANDOZ 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 TOBRADEX DEXAMETHASONE; TOBRAMYCIN SUSPENSION/DROPS;OPHTHALMIC 0.1%;0.3% Yes Yes AB 1988/08/18 1988/08/18 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
2021/05/14 SUPPL-46(补充) Approval Labeling STANDARD
2021/05/14 SUPPL-44(补充) Approval Labeling STANDARD
2020/04/24 SUPPL-43(补充) Approval Labeling STANDARD
2003/06/23 SUPPL-32(补充) Approval Labeling STANDARD
2002/12/11 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
2002/12/04 SUPPL-30(补充) Approval Manufacturing (CMC) STANDARD
2002/08/16 SUPPL-29(补充) Approval Manufacturing (CMC) STANDARD
2001/04/02 SUPPL-27(补充) Approval Manufacturing (CMC) STANDARD
2001/03/16 SUPPL-28(补充) Approval Manufacturing (CMC) STANDARD
2000/06/20 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
2000/02/18 SUPPL-26(补充) Approval Manufacturing (CMC) STANDARD
2000/02/04 SUPPL-24(补充) Approval Manufacturing (CMC) STANDARD
1999/08/17 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
1999/04/28 SUPPL-17(补充) Approval Labeling STANDARD
1999/04/07 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
1999/03/11 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1999/02/05 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
1998/08/04 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1998/02/11 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1997/09/09 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1997/07/31 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1996/09/27 SUPPL-14(补充) Approval Labeling STANDARD
1996/09/27 SUPPL-13(补充) Approval Labeling STANDARD
1996/09/27 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1996/03/18 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1995/11/01 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1995/11/01 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1995/08/03 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1994/10/27 SUPPL-7(补充) Approval Labeling STANDARD
1993/08/31 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1991/12/31 SUPPL-6(补充) Approval Labeling
1991/12/31 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1988/08/18 ORIG-1(原始申请) Approval Type 4 - New Combination 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
001 5149694 2009/09/22 U-923 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
与本品治疗等效的药品
活性成分:DEXAMETHASONE; TOBRAMYCIN 剂型/给药途径:SUSPENSION/DROPS;OPHTHALMIC 规格:0.1%;0.3% 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
050592 001 NDA TOBRADEX DEXAMETHASONE; TOBRAMYCIN SUSPENSION/DROPS;OPHTHALMIC 0.1%;0.3% Prescription Yes Yes AB 1988/08/18 SANDOZ
064134 001 ANDA TOBRAMYCIN AND DEXAMETHASONE DEXAMETHASONE; TOBRAMYCIN SUSPENSION/DROPS;OPHTHALMIC 0.1%;0.3% Prescription No No AB 1999/10/27 BAUSCH AND LOMB
212991 001 ANDA TOBRAMYCIN AND DEXAMETHASONE DEXAMETHASONE; TOBRAMYCIN SUSPENSION/DROPS;OPHTHALMIC 0.1%;0.3% Discontinued No No AB 2021/07/15 AMNEAL
212715 001 ANDA TOBRAMYCIN AND DEXAMETHASONE DEXAMETHASONE; TOBRAMYCIN SUSPENSION/DROPS;OPHTHALMIC 0.1%;0.3% Prescription No No AB 2022/02/11 PADAGIS US
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