药品注册申请号:017386
申请类型:NDA (新药申请)
申请人:I3 PHARMS
申请人全名:I3 PHARMACEUTICALS 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001 ZAROXOLYN METOLAZONE TABLET;ORAL 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1973/11/27 Approved Prior to Jan 1, 1982 Discontinued
002 ZAROXOLYN METOLAZONE TABLET;ORAL 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None Approved Prior to Jan 1, 1982 Discontinued
003 ZAROXOLYN METOLAZONE TABLET;ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None Approved Prior to Jan 1, 1982 Discontinued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
2019/05/24 SUPPL-43(补充) Approval Manufacturing (CMC) STANDARD
2015/03/30 SUPPL-40(补充) Approval Manufacturing (CMC) STANDARD
2013/11/22 SUPPL-39(补充) Approval Manufacturing (CMC) STANDARD
2003/08/19 SUPPL-36(补充) Approval Labeling STANDARD
2002/10/29 SUPPL-34(补充) Approval Labeling STANDARD
2002/04/15 SUPPL-33(补充) Approval Manufacturing (CMC) STANDARD
2001/10/18 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
2001/08/10 SUPPL-32(补充) Approval Labeling STANDARD
1999/08/13 SUPPL-30(补充) Approval Labeling STANDARD
1997/07/14 SUPPL-29(补充) Approval Manufacturing (CMC) STANDARD
1997/01/07 SUPPL-27(补充) Approval Manufacturing (CMC) STANDARD
1995/05/23 SUPPL-26(补充) Approval Labeling STANDARD
1994/05/04 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
1994/01/13 SUPPL-24(补充) Approval Labeling STANDARD
1993/01/13 SUPPL-23(补充) Approval Labeling STANDARD
1989/10/10 SUPPL-22(补充) Approval Labeling
1989/09/12 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1988/12/09 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
1988/02/01 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1987/09/30 SUPPL-15(补充) Approval Labeling
1987/08/26 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1985/08/12 SUPPL-18(补充) Approval Labeling
1984/02/07 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1984/02/07 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1983/07/15 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1983/07/15 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1983/02/18 SUPPL-14(补充) Approval Labeling
1982/12/02 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1982/12/02 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1980/01/03 SUPPL-8(补充) Approval Labeling
1978/04/25 SUPPL-5(补充) Approval Labeling
1978/04/25 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1977/05/11 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1973/11/27 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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