药品注册申请号:019008
申请类型:NDA (新药申请)
申请人:HOSPIRA INC
申请人全名:HOSPIRA 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 BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER BRETYLIUM TOSYLATE INJECTABLE;INJECTION 800MG/100ML No No None 1986/04/16 1986/04/29 Discontinued
002 BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER BRETYLIUM TOSYLATE INJECTABLE;INJECTION 200MG/100ML No No None 1986/04/29 Discontinued
003 BRETYLIUM TOSYLATE IN DEXTROSE 5% IN PLASTIC CONTAINER BRETYLIUM TOSYLATE INJECTABLE;INJECTION 400MG/100ML No No None 1986/04/29 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
2001/06/29 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
1999/04/16 SUPPL-19(补充) Approval Labeling STANDARD
1998/11/05 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1997/06/12 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1997/03/18 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1996/06/26 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1996/02/02 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1995/08/03 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1994/03/04 SUPPL-12(补充) Approval Labeling STANDARD
1991/12/31 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1991/07/18 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1990/03/23 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1990/03/20 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1988/11/22 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1987/09/16 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1987/08/26 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1987/03/13 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1986/10/29 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1986/09/24 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1986/08/08 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1986/04/16 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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