药品注册申请号:050596
申请类型:NDA (新药申请)
申请人:STERIMAX
申请人全名:STERIMAX INC
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 CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 20MG BASE/ML No No None 1985/05/20 1985/05/20 Discontinued
002 CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 20MG BASE/ML No No None 1985/05/20 Discontinued
003 CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 40MG BASE/ML No No None 1985/05/20 Discontinued
004 CLAFORAN IN DEXTROSE 5% IN PLASTIC CONTAINER CEFOTAXIME SODIUM INJECTABLE;INJECTION EQ 40MG BASE/ML No No None 1985/05/20 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
2015/03/23 SUPPL-42(补充) Approval Labeling STANDARD Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs.
2014/04/21 SUPPL-41(补充) Approval Manufacturing (CMC) STANDARD
2014/02/21 SUPPL-40(补充) Approval Labeling STANDARD
2013/05/03 SUPPL-39(补充) Approval Manufacturing (CMC) STANDARD
2011/09/09 SUPPL-37(补充) Approval Labeling STANDARD
2009/05/27 SUPPL-36(补充) Approval Labeling STANDARD
2008/02/21 SUPPL-35(补充) Approval Labeling STANDARD
2004/09/02 SUPPL-31(补充) Approval Labeling STANDARD
2004/06/23 SUPPL-30(补充) Approval Labeling STANDARD
2002/01/18 SUPPL-23(补充) Approval Labeling STANDARD
2001/09/06 SUPPL-28(补充) Approval Manufacturing (CMC) STANDARD
2001/07/27 SUPPL-27(补充) Approval Manufacturing (CMC) STANDARD
2001/04/12 SUPPL-26(补充) Approval Manufacturing (CMC) STANDARD
2001/04/10 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
2000/02/18 SUPPL-24(补充) Approval Manufacturing (CMC) STANDARD
1997/04/24 SUPPL-22(补充) Approval Labeling STANDARD
1996/12/23 SUPPL-20(补充) Approval Labeling STANDARD
1996/09/24 SUPPL-10(补充) Approval Labeling
1996/04/30 SUPPL-18(补充) Approval Labeling STANDARD
1994/11/22 SUPPL-13(补充) Approval Labeling STANDARD
1994/09/14 SUPPL-16(补充) Approval Labeling STANDARD
1994/09/02 SUPPL-17(补充) Approval Labeling STANDARD
1994/06/16 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1994/05/19 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1992/08/10 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1992/03/05 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1989/08/07 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1985/09/23 SUPPL-2(补充) Approval Labeling
1985/07/23 SUPPL-3(补充) Approval Labeling
1985/06/13 SUPPL-1(补充) Approval Labeling
1985/05/20 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)
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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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