药品注册申请号:018030
申请类型:NDA (新药申请)
申请人:B BRAUN
申请人全名:B BRAUN MEDICAL 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 DEXTROSE 2.5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER DEXTROSE; SODIUM CHLORIDE INJECTABLE;INJECTION 2.5GM/100ML;450MG/100ML No No None 1978/02/24 Approved Prior to Jan 1, 1982 Discontinued
002 DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER DEXTROSE; SODIUM CHLORIDE INJECTABLE;INJECTION 5GM/100ML;450MG/100ML No No None Approved Prior to Jan 1, 1982 Discontinued
003 DEXTROSE 5% AND SODIUM CHLORIDE 0.33% IN PLASTIC CONTAINER DEXTROSE; SODIUM CHLORIDE INJECTABLE;INJECTION 5GM/100ML;330MG/100ML No No None Approved Prior to Jan 1, 1982 Discontinued
004 DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER DEXTROSE; SODIUM CHLORIDE INJECTABLE;INJECTION 5GM/100ML;200MG/100ML No No None Approved Prior to Jan 1, 1982 Discontinued
005 DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER DEXTROSE; SODIUM CHLORIDE INJECTABLE;INJECTION 5GM/100ML;110MG/100ML No 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
1990/09/11 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1986/02/18 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1985/06/24 SUPPL-18(补充) Approval Labeling STANDARD
1985/05/17 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1985/04/15 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1985/04/03 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1983/01/24 SUPPL-12(补充) Approval Labeling STANDARD
1981/10/26 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1980/10/24 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1980/08/06 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1980/07/16 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1980/02/12 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1979/10/16 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1979/10/09 SUPPL-7(补充) Approval Labeling STANDARD
1979/06/08 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1978/09/29 SUPPL-3(补充) Approval Labeling STANDARD
1978/09/29 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1978/09/26 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1978/03/31 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1978/02/24 ORIG-1(原始申请) Approval Type 5 - New Formulation or New Manufacturer 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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