药品注册申请号:018538
申请类型:NDA (新药申请)
申请人:SANOFI AVENTIS US
申请人全名:SANOFI AVENTIS US 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001 LOZOL INDAPAMIDE TABLET;ORAL 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1983/07/06 1983/07/06 Discontinued
002 LOZOL INDAPAMIDE TABLET;ORAL 1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1993/04/29 Discontinued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
2021/03/02 SUPPL-30(补充) Approval Labeling STANDARD
2009/09/03 SUPPL-28(补充) Approval Labeling STANDARD
2000/10/10 SUPPL-26(补充) Approval Labeling STANDARD
2000/03/07 SUPPL-27(补充) Approval Manufacturing (CMC) STANDARD
1998/12/11 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
1998/01/27 SUPPL-24(补充) Approval Manufacturing (CMC) STANDARD
1996/10/29 SUPPL-21(补充) Approval Labeling STANDARD
1996/10/29 SUPPL-20(补充) Approval Labeling STANDARD
1996/05/16 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
1996/02/26 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
1993/08/19 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1993/04/29 SUPPL-17(补充) Approval Efficacy
1993/03/31 SUPPL-19(补充) Approval Labeling STANDARD
1992/06/24 SUPPL-16(补充) Approval Labeling
1992/06/23 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1992/04/01 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1991/09/25 SUPPL-14(补充) Approval Labeling
1990/03/08 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1990/01/03 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1989/10/13 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1989/07/10 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1989/02/23 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1988/11/29 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1988/11/09 SUPPL-6(补充) Approval Labeling
1988/07/08 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1987/06/30 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1984/04/10 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1983/11/29 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1983/10/12 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1983/07/06 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity STANDARD
与本品相关的专利信息(来自FDA橙皮书Orange Book)
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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
本品无治疗等效药品
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