药品注册申请号:018598
申请类型:NDA (新药申请)
申请人:FOSUN PHARMA
申请人全名:FOSUN PHARMA USA 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
003 SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLE; TRIMETHOPRIM TABLET;ORAL 400MG;80MG No No None 1982/05/19 1982/05/19 Discontinued
004 SULFAMETHOXAZOLE AND TRIMETHOPRIM DOUBLE STRENGTH SULFAMETHOXAZOLE; TRIMETHOPRIM TABLET;ORAL 800MG;160MG No No None 1982/05/19 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
2021/10/15 SUPPL-54(补充) Approval Labeling STANDARD
2019/09/05 SUPPL-52(补充) Approval Labeling STANDARD
2011/02/03 SUPPL-51(补充) Approval Labeling Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs.
2008/02/20 SUPPL-50(补充) Approval Labeling
2000/06/23 SUPPL-41(补充) Approval Manufacturing (CMC)
2000/02/02 SUPPL-40(补充) Approval Manufacturing (CMC)
1998/01/07 SUPPL-36(补充) Approval Labeling
1996/10/08 SUPPL-34(补充) Approval Manufacturing (CMC)
1996/10/08 SUPPL-33(补充) Approval Manufacturing (CMC)
1996/07/11 SUPPL-35(补充) Approval Labeling
1996/05/03 SUPPL-32(补充) Approval Labeling
1996/05/03 SUPPL-30(补充) Approval Manufacturing (CMC)
1995/05/10 SUPPL-28(补充) Approval Manufacturing (CMC)
1995/05/10 SUPPL-27(补充) Approval Manufacturing (CMC)
1994/10/20 SUPPL-17(补充) Approval Manufacturing (CMC)
1994/10/20 SUPPL-16(补充) Approval Manufacturing (CMC)
1994/03/09 SUPPL-19(补充) Approval Labeling
1992/07/28 SUPPL-18(补充) Approval Labeling
1989/03/27 SUPPL-13(补充) Approval Manufacturing (CMC)
1989/03/27 SUPPL-12(补充) Approval Manufacturing (CMC)
1989/03/08 SUPPL-15(补充) Approval Labeling
1988/11/07 SUPPL-14(补充) Approval Labeling
1988/01/13 SUPPL-11(补充) Approval Manufacturing (CMC)
1987/08/18 SUPPL-9(补充) Approval Manufacturing (CMC)
1986/01/07 SUPPL-8(补充) Approval Manufacturing (CMC)
1985/07/29 SUPPL-7(补充) Approval Manufacturing (CMC)
1982/05/19 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)
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与本品相关的市场独占权保护信息
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与本品治疗等效的药品
本品无治疗等效药品
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