药品注册申请号:050051
申请类型:NDA (新药申请)
申请人:WYETH AYERST
申请人全名:WYETH AYERST LABORATORIES
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 GRISACTIN GRISEOFULVIN, MICROCRYSTALLINE CAPSULE;ORAL 250MG No No None 1962/08/22 Approved Prior to Jan 1, 1982 Discontinued
002 GRISACTIN GRISEOFULVIN, MICROCRYSTALLINE CAPSULE;ORAL 125MG 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
1996/05/09 SUPPL-65(补充) Approval Manufacturing (CMC)
1993/01/28 SUPPL-5(补充) Approval Manufacturing (CMC)
1987/07/29 SUPPL-4(补充) Approval Manufacturing (CMC)
1984/01/12 SUPPL-2(补充) Approval Manufacturing (CMC)
1983/06/29 SUPPL-1(补充) Approval Manufacturing (CMC)
1981/05/26 SUPPL-64(补充) Approval Manufacturing (CMC)
1981/05/20 SUPPL-63(补充) Approval Manufacturing (CMC)
1981/02/19 SUPPL-62(补充) Approval Manufacturing (CMC)
1980/12/31 SUPPL-61(补充) Approval Manufacturing (CMC)
1980/08/27 SUPPL-60(补充) Approval Manufacturing (CMC)
1980/06/24 SUPPL-59(补充) Approval Manufacturing (CMC)
1980/01/21 SUPPL-58(补充) Approval Manufacturing (CMC)
1979/11/08 SUPPL-57(补充) Approval Manufacturing (CMC)
1979/11/08 SUPPL-56(补充) Approval Manufacturing (CMC)
1978/10/18 SUPPL-55(补充) Approval Manufacturing (CMC)
1977/06/21 SUPPL-54(补充) Approval Manufacturing (CMC)
1977/06/10 SUPPL-53(补充) Approval Manufacturing (CMC)
1976/10/29 SUPPL-52(补充) Approval Manufacturing (CMC)
1976/05/13 SUPPL-50(补充) Approval Manufacturing (CMC)
1976/04/01 SUPPL-49(补充) Approval Manufacturing (CMC)
1975/11/11 SUPPL-48(补充) Approval Manufacturing (CMC)
1975/09/30 SUPPL-47(补充) Approval Manufacturing (CMC)
1974/10/16 SUPPL-51(补充) Approval Manufacturing (CMC)
1974/06/05 SUPPL-46(补充) Approval Manufacturing (CMC)
1974/05/22 SUPPL-45(补充) Approval Manufacturing (CMC)
1974/02/22 SUPPL-44(补充) Approval Manufacturing (CMC)
1973/02/12 SUPPL-43(补充) Approval Manufacturing (CMC)
1973/02/02 SUPPL-42(补充) Approval Manufacturing (CMC)
1972/06/20 SUPPL-37(补充) Approval Manufacturing (CMC)
1972/06/16 SUPPL-41(补充) Approval Labeling
1972/05/03 SUPPL-40(补充) Approval Labeling
1972/03/27 SUPPL-39(补充) Approval Manufacturing (CMC)
1972/02/03 SUPPL-38(补充) Approval Manufacturing (CMC)
1971/11/12 SUPPL-35(补充) Approval Labeling
1971/09/13 SUPPL-34(补充) Approval Labeling
1971/06/28 SUPPL-33(补充) Approval Labeling
1971/06/03 SUPPL-32(补充) Approval Manufacturing (CMC)
1969/07/29 SUPPL-31(补充) Approval Manufacturing (CMC)
1969/07/15 SUPPL-30(补充) Approval Manufacturing (CMC)
1969/07/15 SUPPL-29(补充) Approval Manufacturing (CMC)
1969/04/24 SUPPL-28(补充) Approval Manufacturing (CMC)
1967/07/27 SUPPL-27(补充) Approval Labeling
1966/10/28 SUPPL-25(补充) Approval Manufacturing (CMC)
1966/09/27 SUPPL-24(补充) Approval Manufacturing (CMC)
1966/05/16 SUPPL-23(补充) Approval Manufacturing (CMC)
1966/05/02 SUPPL-21(补充) Approval Labeling
1966/05/02 SUPPL-20(补充) Approval Labeling
1966/04/29 SUPPL-22(补充) Approval Labeling
1966/03/18 SUPPL-19(补充) Approval Labeling
1966/03/15 SUPPL-18(补充) Approval Manufacturing (CMC)
1966/03/14 SUPPL-17(补充) Approval Manufacturing (CMC)
1966/02/07 SUPPL-16(补充) Approval Labeling
1965/11/02 SUPPL-15(补充) Approval Labeling
1965/04/26 SUPPL-14(补充) Approval Manufacturing (CMC)
1965/03/16 SUPPL-9(补充) Approval Labeling
1964/11/24 SUPPL-13(补充) Approval Manufacturing (CMC)
1964/09/21 SUPPL-11(补充) Approval Labeling
1964/08/04 SUPPL-7(补充) Approval Labeling
1964/06/24 SUPPL-10(补充) Approval Manufacturing (CMC)
1962/08/22 ORIG-1(原始申请) Approval
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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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