药品注册申请号:018827
申请类型:NDA (新药申请)
申请人:ORGANON
申请人全名:ORGANON LLC A SUB OF ORGANON AND CO
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 LOTRISONE BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE CREAM;TOPICAL EQ 0.05% BASE;1% Yes No AB 1984/07/10 1984/07/10 Discontinued
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
2019/06/14 SUPPL-50(补充) Approval Labeling STANDARD
2018/05/21 SUPPL-49(补充) Approval Labeling STANDARD
2014/04/21 SUPPL-46(补充) Approval Labeling STANDARD
2009/05/11 SUPPL-42(补充) Approval Labeling STANDARD
2008/01/25 SUPPL-38(补充) Approval Labeling STANDARD
2003/03/27 SUPPL-25(补充) Approval Labeling STANDARD
2002/01/10 SUPPL-24(补充) Approval Manufacturing (CMC) STANDARD
2001/10/03 SUPPL-22(补充) Approval Efficacy STANDARD
2001/10/03 SUPPL-20(补充) Approval Labeling STANDARD
2001/10/03 SUPPL-9(补充) Approval Labeling
2001/10/03 SUPPL-7(补充) Approval Labeling
2001/02/28 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
2000/02/02 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1999/05/14 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1998/11/10 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1998/07/31 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1998/06/15 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1998/05/18 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1995/01/30 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1995/01/30 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1994/10/06 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1990/09/11 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1990/08/01 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1987/10/29 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1986/09/12 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1986/05/20 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1986/04/23 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1985/02/22 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1984/07/10 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
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:BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE 剂型/给药途径:CREAM;TOPICAL 规格:EQ 0.05% BASE;1% 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
018827 001 NDA LOTRISONE BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE CREAM;TOPICAL EQ 0.05% BASE;1% Discontinued Yes No AB 1984/07/10 ORGANON
075673 001 ANDA CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE CREAM;TOPICAL EQ 0.05% BASE;1% Prescription No Yes AB 2001/05/29 TARO
075502 001 ANDA CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE CREAM;TOPICAL EQ 0.05% BASE;1% Prescription No No AB 2001/06/05 FOUGERA PHARMS
076002 001 ANDA CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE CREAM;TOPICAL EQ 0.05% BASE;1% Prescription No No AB 2002/08/02 ACTAVIS MID ATLANTIC
202894 001 ANDA CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE CREAM;TOPICAL EQ 0.05% BASE;1% Prescription No No AB 2015/10/30 GLENMARK PHARMS
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