药品注册申请号:071210
申请类型:ANDA (仿制药申请)
申请人:CHARTWELL RX
申请人全名:CHARTWELL RX SCIENCES 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 HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG No No AB 1988/03/11 1988/03/11 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
2017/02/23 SUPPL-33(补充) Approval Labeling STANDARD
2010/12/06 SUPPL-29(补充) Approval Labeling
2009/07/16 SUPPL-27(补充) Approval Labeling
2008/09/08 SUPPL-26(补充) Approval Labeling
2008/05/29 SUPPL-23(补充) Approval Labeling
2008/04/02 SUPPL-22(补充) Approval Labeling
2002/12/11 SUPPL-19(补充) Approval Manufacturing (CMC)
2002/12/11 SUPPL-18(补充) Approval Manufacturing (CMC)
2002/12/11 SUPPL-17(补充) Approval Manufacturing (CMC)
2002/09/05 SUPPL-16(补充) Approval Labeling
2001/10/16 SUPPL-12(补充) Approval Labeling
2001/06/28 SUPPL-13(补充) Approval Manufacturing (CMC)
2001/06/14 SUPPL-14(补充) Approval Manufacturing (CMC)
2001/05/09 SUPPL-15(补充) Approval Manufacturing (CMC)
2000/10/31 SUPPL-11(补充) Approval Manufacturing (CMC)
2000/04/04 SUPPL-10(补充) Approval Manufacturing (CMC)
2000/01/06 SUPPL-8(补充) Approval Manufacturing (CMC)
1999/05/05 SUPPL-9(补充) Approval Manufacturing (CMC)
1998/09/21 SUPPL-7(补充) Approval Labeling
1998/09/21 SUPPL-6(补充) Approval Manufacturing (CMC)
1995/02/02 SUPPL-5(补充) Approval Manufacturing (CMC)
1990/04/20 SUPPL-4(补充) Approval Labeling
1989/06/01 SUPPL-3(补充) Approval Labeling
1988/09/09 SUPPL-2(补充) Approval Labeling
1988/04/26 SUPPL-1(补充) Approval Manufacturing (CMC)
1988/03/11 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:HALOPERIDOL 剂型/给药途径:TABLET;ORAL 规格:10MG 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
071130 003 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 1987/05/12 AIPING PHARM INC
071173 001 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 1988/01/07 INNOGENIX
071210 001 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 1988/03/11 CHARTWELL RX
077580 004 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 2007/11/29 ZYDUS PHARMS USA
070278 002 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 2009/07/16 MYLAN
211061 005 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 2020/01/08 UPSHER SMITH LABS
200854 005 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Discontinued No No AB 2022/07/01 ACTAVIS GROUP
216004 005 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 2022/11/18 MSN
216918 005 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 2024/04/11 MANKIND PHARMA
218789 005 ANDA HALOPERIDOL HALOPERIDOL TABLET;ORAL 10MG Prescription No No AB 2024/04/19 AUROBINDO PHARMA LTD
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