药品注册申请号:016909
申请类型:NDA (新药申请)
申请人:ALVOGEN
申请人全名:ALVOGEN 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
002 LIDEX FLUOCINONIDE OINTMENT;TOPICAL 0.05% Yes No AB 1971/09/22 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
2016/06/08 SUPPL-53(补充) Approval Manufacturing (CMC) STANDARD
2005/12/16 SUPPL-49(补充) Approval Manufacturing (CMC) STANDARD
2000/09/26 SUPPL-47(补充) Approval Manufacturing (CMC) STANDARD
1996/07/22 SUPPL-46(补充) Approval Manufacturing (CMC) STANDARD
1992/11/16 SUPPL-45(补充) Approval Manufacturing (CMC) STANDARD
1992/04/24 SUPPL-44(补充) Approval Manufacturing (CMC) STANDARD
1991/03/12 SUPPL-43(补充) Approval Labeling
1990/02/13 SUPPL-42(补充) Approval Manufacturing (CMC) STANDARD
1989/12/06 SUPPL-41(补充) Approval Manufacturing (CMC) STANDARD
1989/09/26 SUPPL-40(补充) Approval Manufacturing (CMC) STANDARD
1989/02/10 SUPPL-39(补充) Approval Manufacturing (CMC) STANDARD
1984/08/29 SUPPL-38(补充) Approval Manufacturing (CMC) STANDARD
1984/05/16 SUPPL-37(补充) Approval Manufacturing (CMC) STANDARD
1983/09/07 SUPPL-36(补充) Approval Manufacturing (CMC) STANDARD
1983/04/21 SUPPL-35(补充) Approval Labeling
1982/11/19 SUPPL-33(补充) Approval Manufacturing (CMC) STANDARD
1981/11/20 SUPPL-32(补充) Approval Manufacturing (CMC) STANDARD
1981/11/10 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
1981/03/24 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
1981/01/19 SUPPL-30(补充) Approval Manufacturing (CMC) STANDARD
1981/01/19 SUPPL-29(补充) Approval Manufacturing (CMC) STANDARD
1981/01/19 SUPPL-28(补充) Approval Manufacturing (CMC) STANDARD
1981/01/19 SUPPL-27(补充) Approval Manufacturing (CMC) STANDARD
1980/08/07 SUPPL-26(补充) Approval Manufacturing (CMC) STANDARD
1979/10/23 SUPPL-24(补充) Approval Manufacturing (CMC) STANDARD
1979/08/13 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
1979/01/02 SUPPL-20(补充) Approval Labeling
1978/11/30 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1978/11/29 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
1978/11/07 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
1978/07/05 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1978/04/11 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1977/12/14 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1977/06/04 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1977/01/11 SUPPL-14(补充) Approval Labeling
1971/09/22 ORIG-1(原始申请) Approval Type 3 - New Dosage Form 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
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:FLUOCINONIDE 剂型/给药途径:OINTMENT;TOPICAL 规格:0.05% 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
016909 002 NDA LIDEX FLUOCINONIDE OINTMENT;TOPICAL 0.05% Prescription Yes No AB Approved Prior to Jan 1, 1982 ALVOGEN
073481 001 ANDA FLUOCINONIDE FLUOCINONIDE OINTMENT;TOPICAL 0.05% Prescription No No AB 1991/12/27 TEVA
074905 001 ANDA FLUOCINONIDE FLUOCINONIDE OINTMENT;TOPICAL 0.05% Prescription No No AB 1997/08/26 FOUGERA PHARMS
075008 001 ANDA FLUOCINONIDE FLUOCINONIDE OINTMENT;TOPICAL 0.05% Prescription No Yes AB 1999/06/30 TARO
207538 001 ANDA FLUOCINONIDE FLUOCINONIDE OINTMENT;TOPICAL 0.05% Prescription No No AB 2017/07/31 CHARTWELL RX
207680 001 ANDA FLUOCINONIDE FLUOCINONIDE OINTMENT;TOPICAL 0.05% Discontinued No No AB 2018/09/28 PAI HOLDINGS PHARM
212976 001 ANDA FLUOCINONIDE FLUOCINONIDE OINTMENT;TOPICAL 0.05% Prescription No No AB 2019/11/26 XIROMED
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