药品注册申请号:084092
申请类型:ANDA (仿制药申请)
申请人:INVATECH
申请人全名:INVATECH PHARMA SOLUTIONS 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
003 MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG No No AA 1975/03/19 1989/05/22 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
2007/06/19 SUPPL-106(补充) Approval Manufacturing (CMC)
2002/03/25 SUPPL-100(补充) Approval Manufacturing (CMC)
2002/01/22 SUPPL-99(补充) Approval Manufacturing (CMC)
2001/04/18 SUPPL-98(补充) Approval Manufacturing (CMC)
1999/05/05 SUPPL-97(补充) Approval Manufacturing (CMC)
1999/02/11 SUPPL-96(补充) Approval Manufacturing (CMC)
1999/02/11 SUPPL-95(补充) Approval Manufacturing (CMC)
1999/02/11 SUPPL-94(补充) Approval Manufacturing (CMC)
1999/02/11 SUPPL-93(补充) Approval Labeling
1996/04/23 SUPPL-90(补充) Approval Manufacturing (CMC)
1995/11/07 SUPPL-91(补充) Approval Manufacturing (CMC)
1989/05/22 SUPPL-87(补充) Approval Labeling
1987/01/28 SUPPL-82(补充) Approval Manufacturing (CMC)
1986/04/24 SUPPL-85(补充) Approval Manufacturing (CMC)
1985/03/01 SUPPL-80(补充) Approval Manufacturing (CMC)
1984/03/15 SUPPL-79(补充) Approval Manufacturing (CMC)
1984/03/15 SUPPL-77(补充) Approval Manufacturing (CMC)
1984/03/15 SUPPL-76(补充) Approval Manufacturing (CMC)
1984/03/15 SUPPL-75(补充) Approval Manufacturing (CMC)
1984/03/15 SUPPL-74(补充) Approval Manufacturing (CMC)
1984/01/25 SUPPL-72(补充) Approval Manufacturing (CMC)
1982/05/13 SUPPL-58(补充) Approval Manufacturing (CMC)
1982/05/13 SUPPL-57(补充) Approval Manufacturing (CMC)
1982/05/13 SUPPL-56(补充) Approval Manufacturing (CMC)
1982/03/11 SUPPL-71(补充) Approval Manufacturing (CMC)
1982/03/11 SUPPL-70(补充) Approval Manufacturing (CMC)
1982/03/11 SUPPL-69(补充) Approval Manufacturing (CMC)
1982/03/11 SUPPL-68(补充) Approval Manufacturing (CMC)
1975/03/19 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:MECLIZINE HYDROCHLORIDE 剂型/给药途径:TABLET;ORAL 规格:25MG 治疗等效代码:AA
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
084657 001 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Discontinued No No AA Approved Prior to Jan 1, 1982 ANI PHARMS
087128 001 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No No AA Approved Prior to Jan 1, 1982 APNAR PHARMA LP
010721 004 NDA ANTIVERT MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription Yes No AA Approved Prior to Jan 1, 1982 CASPER PHARMA LLC
084092 003 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No No AA 1989/05/22 INVATECH
040659 002 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No No AA 2010/06/04 JUBILANT CADISTA
201451 002 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No Yes AA 2011/02/23 AMNEAL PHARMS
200294 002 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No No AA 2012/04/13 EPIC PHARMA LLC
202640 002 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No No AA 2012/09/17 AUROBINDO PHARMA USA
205136 002 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No No AA 2019/02/22 WILSHIRE PHARMS INC
213957 002 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No No AA 2020/06/23 ZYDUS LIFESCIENCES
200432 002 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Discontinued No No AA 2022/02/17 INVAGEN PHARMS
203003 002 ANDA MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET;ORAL 25MG Prescription No No AA 2022/08/11 CHARTWELL RX
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