药品注册申请号:018840
申请类型:NDA (新药申请)
申请人:BAXTER HLTHCARE
申请人全名:BAXTER HEALTHCARE CORP
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 5% AND ELECTROLYTE NO. 75 IN PLASTIC CONTAINER DEXTROSE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM CHLORIDE; SODIUM LACTATE INJECTABLE;INJECTION 5GM/100ML;205MG/100ML;100MG/100ML;120MG/100ML;220MG/100ML No No None 1983/06/29 1983/06/29 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
2005/08/26 SUPPL-29(补充) Approval Manufacturing (CMC) STANDARD
2005/06/07 SUPPL-28(补充) Approval Labeling STANDARD
2001/08/14 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
2000/11/29 SUPPL-23(补充) Approval Labeling STANDARD
1999/11/24 SUPPL-24(补充) Approval Manufacturing (CMC) STANDARD
1997/04/29 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
1994/09/30 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1994/02/18 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
1991/04/29 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1991/04/26 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1991/03/26 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1991/02/15 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1989/07/26 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1989/01/12 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1987/07/25 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1987/05/28 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1986/02/27 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1985/06/24 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1985/06/13 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1985/04/26 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1985/04/17 SUPPL-4(补充) Approval Labeling STANDARD
1984/09/22 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1983/06/29 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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