药品注册申请号:070028
申请类型:ANDA (仿制药申请)
申请人:ANI PHARMS
申请人全名:ANI PHARMACEUTICALS 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 SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLE; TRIMETHOPRIM SUSPENSION;ORAL 200MG/5ML;40MG/5ML No No None 1985/10/29 1987/06/02 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
2024/06/24 SUPPL-34(补充) Approval Labeling STANDARD
2022/09/22 SUPPL-33(补充) Approval Labeling STANDARD
2022/09/22 SUPPL-32(补充) Approval Labeling STANDARD
2002/05/31 SUPPL-31(补充) Approval Manufacturing (CMC)
2001/05/29 SUPPL-28(补充) Approval Manufacturing (CMC)
2000/08/30 SUPPL-29(补充) Approval Labeling
1999/12/02 SUPPL-26(补充) Approval Manufacturing (CMC)
1999/12/02 SUPPL-25(补充) Approval Manufacturing (CMC)
1999/02/12 SUPPL-22(补充) Approval Manufacturing (CMC)
1999/02/12 SUPPL-21(补充) Approval Manufacturing (CMC)
1998/08/04 SUPPL-20(补充) Approval Labeling
1998/01/30 SUPPL-19(补充) Approval Labeling
1997/05/09 SUPPL-18(补充) Approval Manufacturing (CMC)
1996/02/22 SUPPL-16(补充) Approval Manufacturing (CMC)
1994/07/07 SUPPL-15(补充) Approval Manufacturing (CMC)
1994/07/07 SUPPL-14(补充) Approval Manufacturing (CMC)
1994/07/07 SUPPL-13(补充) Approval Manufacturing (CMC)
1994/07/07 SUPPL-12(补充) Approval Manufacturing (CMC)
1994/07/07 SUPPL-11(补充) Approval Manufacturing (CMC)
1994/07/07 SUPPL-10(补充) Approval Manufacturing (CMC)
1994/07/07 SUPPL-9(补充) Approval Labeling
1990/12/20 SUPPL-8(补充) Approval Manufacturing (CMC)
1990/12/20 SUPPL-7(补充) Approval Manufacturing (CMC)
1990/12/20 SUPPL-6(补充) Approval Manufacturing (CMC)
1990/06/28 SUPPL-5(补充) Approval Labeling
1990/06/28 SUPPL-4(补充) Approval Labeling
1987/04/28 SUPPL-1(补充) Approval Manufacturing (CMC)
1985/10/29 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
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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