药品注册申请号:017637
申请类型:NDA (新药申请)
申请人:ICU MEDICAL INC
申请人全名:ICU 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
002 PHYSIOSOL IN PLASTIC CONTAINER MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE SOLUTION;IRRIGATION 30MG/100ML;37MG/100ML;222MG/100ML;526MG/100ML;502MG/100ML No No None 1978/02/08 1982/07/08 Prescription
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
2014/06/12 SUPPL-61(补充) Approval Manufacturing (CMC) STANDARD
2000/02/23 SUPPL-46(补充) Approval Labeling STANDARD
1999/06/04 SUPPL-47(补充) Approval Manufacturing (CMC) STANDARD
1998/05/12 SUPPL-44(补充) Approval Labeling STANDARD
1998/02/04 SUPPL-45(补充) Approval Manufacturing (CMC) STANDARD
1996/08/27 SUPPL-43(补充) Approval Manufacturing (CMC) STANDARD
1993/08/24 SUPPL-40(补充) Approval Manufacturing (CMC) STANDARD
1992/06/30 SUPPL-41(补充) Approval Manufacturing (CMC) STANDARD
1988/11/25 SUPPL-39(补充) Approval Manufacturing (CMC) STANDARD
1986/01/31 SUPPL-38(补充) Approval Manufacturing (CMC) STANDARD
1986/01/18 SUPPL-35(补充) Approval Manufacturing (CMC) STANDARD
1985/10/29 SUPPL-37(补充) Approval Manufacturing (CMC) STANDARD
1984/11/09 SUPPL-34(补充) Approval Manufacturing (CMC) STANDARD
1984/10/22 SUPPL-33(补充) Approval Manufacturing (CMC) STANDARD
1984/08/25 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
1984/03/15 SUPPL-30(补充) Approval Manufacturing (CMC) STANDARD
1984/03/01 SUPPL-28(补充) Approval Manufacturing (CMC) STANDARD
1982/07/08 SUPPL-25(补充) Approval Labeling
1982/06/18 SUPPL-29(补充) Approval Manufacturing (CMC) STANDARD
1982/06/10 SUPPL-27(补充) Approval Manufacturing (CMC) STANDARD
1981/11/06 SUPPL-26(补充) Approval Manufacturing (CMC) STANDARD
1981/07/21 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1980/10/01 SUPPL-24(补充) Approval Labeling
1980/09/08 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
1980/06/06 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
1980/06/06 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1980/05/23 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1980/03/20 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1979/10/04 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1979/07/31 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1979/07/18 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1979/04/30 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1979/02/02 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1979/01/05 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1978/12/01 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1978/11/22 SUPPL-7(补充) Approval Labeling
1978/11/22 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1978/09/08 SUPPL-5(补充) Approval Labeling
1978/09/08 SUPPL-2(补充) Approval Labeling
1978/08/29 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1978/06/30 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1978/02/08 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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