药品注册申请号:004570
申请类型:NDA (新药申请)
申请人:PHARMACIA AND UPJOHN
申请人全名:PHARMACIA AND UPJOHN CO
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 HEPARIN SODIUM HEPARIN SODIUM INJECTABLE;INJECTION 1,000 UNITS/ML No No None 1942/02/05 Approved Prior to Jan 1, 1982 Discontinued
002 HEPARIN SODIUM HEPARIN SODIUM INJECTABLE;INJECTION 5,000 UNITS/ML No No None Approved Prior to Jan 1, 1982 Discontinued
003 HEPARIN SODIUM HEPARIN SODIUM INJECTABLE;INJECTION 10,000 UNITS/ML 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
2000/04/03 SUPPL-56(补充) Approval Manufacturing (CMC)
1999/09/15 SUPPL-55(补充) Approval Labeling STANDARD
1996/03/04 SUPPL-54(补充) Approval Labeling STANDARD
1996/01/31 SUPPL-53(补充) Approval Manufacturing (CMC)
1991/07/09 SUPPL-52(补充) Approval Manufacturing (CMC)
1990/01/29 SUPPL-49(补充) Approval Manufacturing (CMC)
1988/11/16 SUPPL-51(补充) Approval Labeling
1988/08/12 SUPPL-50(补充) Approval Labeling
1988/01/29 SUPPL-46(补充) Approval Manufacturing (CMC)
1987/07/24 SUPPL-48(补充) Approval Labeling
1987/01/21 SUPPL-47(补充) Approval Labeling
1986/10/24 SUPPL-43(补充) Approval Labeling
1983/03/25 SUPPL-45(补充) Approval Labeling
1983/01/21 SUPPL-44(补充) Approval Labeling
1981/08/19 SUPPL-42(补充) Approval Labeling
1981/06/02 SUPPL-41(补充) Approval Labeling
1981/06/02 SUPPL-33(补充) Approval Labeling
1981/02/18 SUPPL-35(补充) Approval Labeling
1981/02/04 SUPPL-40(补充) Approval Labeling
1981/01/14 SUPPL-39(补充) Approval Labeling
1980/12/03 SUPPL-38(补充) Approval Manufacturing (CMC)
1980/10/14 SUPPL-36(补充) Approval Manufacturing (CMC)
1980/08/20 SUPPL-37(补充) Approval Manufacturing (CMC)
1980/02/05 SUPPL-34(补充) Approval Manufacturing (CMC)
1980/02/05 SUPPL-32(补充) Approval Manufacturing (CMC)
1980/02/05 SUPPL-31(补充) Approval Manufacturing (CMC)
1978/10/04 SUPPL-29(补充) Approval Manufacturing (CMC)
1978/02/02 SUPPL-26(补充) Approval Manufacturing (CMC)
1977/02/11 SUPPL-23(补充) Approval Manufacturing (CMC)
1976/07/09 SUPPL-20(补充) Approval Manufacturing (CMC)
1976/02/24 SUPPL-22(补充) Approval Labeling
1976/02/24 SUPPL-21(补充) Approval Labeling
1975/08/14 SUPPL-19(补充) Approval Labeling
1975/08/14 SUPPL-18(补充) Approval Manufacturing (CMC)
1942/02/05 ORIG-1(原始申请) Approval UNKNOWN
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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