药品注册申请号:084108
申请类型:ANDA (仿制药申请)
申请人:ALCON LABS INC
申请人全名:ALCON LABORATORIES 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 CYCLOGYL CYCLOPENTOLATE HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC 2% Yes Yes AT 1974/07/31 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
2003/10/31 SUPPL-35(补充) Approval Labeling
2002/12/23 SUPPL-34(补充) Approval Manufacturing (CMC)
2002/10/11 SUPPL-33(补充) Approval Manufacturing (CMC)
2001/11/20 SUPPL-32(补充) Approval Manufacturing (CMC)
2000/04/28 SUPPL-30(补充) Approval Manufacturing (CMC)
2000/04/07 SUPPL-31(补充) Approval Manufacturing (CMC)
1999/05/07 SUPPL-28(补充) Approval Manufacturing (CMC)
1999/03/23 SUPPL-29(补充) Approval Manufacturing (CMC)
1999/03/04 SUPPL-26(补充) Approval Manufacturing (CMC)
1998/12/09 SUPPL-27(补充) Approval Manufacturing (CMC)
1998/02/17 SUPPL-25(补充) Approval Manufacturing (CMC)
1997/01/16 SUPPL-20(补充) Approval Labeling
1995/10/05 SUPPL-24(补充) Approval Manufacturing (CMC)
1995/08/04 SUPPL-23(补充) Approval Manufacturing (CMC)
1994/08/04 SUPPL-22(补充) Approval Manufacturing (CMC)
1994/08/03 SUPPL-21(补充) Approval Labeling
1993/12/02 SUPPL-19(补充) Approval Labeling
1993/06/04 SUPPL-16(补充) Approval Manufacturing (CMC)
1993/06/04 SUPPL-15(补充) Approval Manufacturing (CMC)
1992/11/05 SUPPL-18(补充) Approval Manufacturing (CMC)
1992/07/29 SUPPL-17(补充) Approval Labeling
1991/02/20 SUPPL-14(补充) Approval Manufacturing (CMC)
1991/02/20 SUPPL-13(补充) Approval Manufacturing (CMC)
1989/11/20 SUPPL-9(补充) Approval Labeling
1983/12/08 SUPPL-3(补充) Approval Manufacturing (CMC)
1982/10/12 SUPPL-2(补充) Approval Manufacturing (CMC)
1974/07/31 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:CYCLOPENTOLATE HYDROCHLORIDE 剂型/给药途径:SOLUTION/DROPS;OPHTHALMIC 规格:2% 治疗等效代码:AT
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
084108 001 ANDA CYCLOGYL CYCLOPENTOLATE HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC 2% Prescription Yes Yes AT Approved Prior to Jan 1, 1982 ALCON LABS INC
040165 001 ANDA AKPENTOLATE CYCLOPENTOLATE HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC 2% Prescription No No AT 1997/01/13 RISING
更多信息
药品NDC数据与药品包装、标签说明书
©2006-2024 DrugFuture->U.S. FDA Drugs Database