药品注册申请号:076002
申请类型:ANDA (仿制药申请)
申请人:ACTAVIS MID ATLANTIC
申请人全名:ACTAVIS MID ATLANTIC LLC
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 CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE; CLOTRIMAZOLE CREAM;TOPICAL EQ 0.05% BASE;1% No No AB 2002/08/02 2002/08/02 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
2020/07/06 SUPPL-21(补充) Approval Labeling STANDARD
2017/01/23 SUPPL-17(补充) Approval Labeling STANDARD
2008/05/13 SUPPL-7(补充) Approval Labeling
2004/10/20 SUPPL-4(补充) Approval Labeling
2002/08/02 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: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
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