药品注册申请号:018741
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 DIPROLENE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED;TOPICAL EQ 0.05% BASE Yes Yes AB 1983/07/27 1983/07/27 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
2019/05/01 SUPPL-40(补充) Approval Labeling STANDARD
2018/03/28 SUPPL-38(补充) Approval Labeling STANDARD
2014/08/13 SUPPL-36(补充) Approval Labeling STANDARD
2006/08/28 SUPPL-28(补充) Approval Efficacy STANDARD
2005/10/07 SUPPL-16(补充) Approval Labeling
1998/11/10 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
1998/07/31 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1998/06/15 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1998/06/15 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1995/11/30 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1991/11/08 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1990/08/01 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1989/05/24 SUPPL-13(补充) Approval Labeling
1988/11/30 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1987/10/29 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1986/09/29 SUPPL-1(补充) Approval Labeling
1986/09/12 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1986/05/20 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1986/04/23 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1985/02/22 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1984/11/16 SUPPL-3(补充) Approval Labeling
1983/12/15 SUPPL-2(补充) Approval Labeling
1983/07/27 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:BETAMETHASONE DIPROPIONATE 剂型/给药途径:OINTMENT, AUGMENTED;TOPICAL 规格:EQ 0.05% BASE 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
018741 001 NDA DIPROLENE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED;TOPICAL EQ 0.05% BASE Prescription Yes Yes AB 1983/07/27 ORGANON
074304 001 ANDA BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED;TOPICAL EQ 0.05% BASE Prescription No No AB 1995/08/31 ACTAVIS MID ATLANTIC
075373 001 ANDA BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED;TOPICAL EQ 0.05% BASE Prescription No No AB 1999/06/22 FOUGERA PHARMS
076753 001 ANDA BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED;TOPICAL EQ 0.05% BASE Prescription No No AB 2004/10/12 TARO
206118 001 ANDA BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED;TOPICAL EQ 0.05% BASE Discontinued No No AB 2017/11/09 PADAGIS US
209106 001 ANDA BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED;TOPICAL EQ 0.05% BASE Prescription No No AB 2019/12/18 LUPIN LTD
218289 001 ANDA BETAMETHASONE DIPROPIONATE BETAMETHASONE DIPROPIONATE OINTMENT, AUGMENTED;TOPICAL EQ 0.05% BASE Prescription No No AB 2024/04/10 AUROBINDO PHARMA LTD
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