药品注册申请号:050324
申请类型:NDA (新药申请)
申请人:MERCK
申请人全名:MERCK AND CO 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 NEODECADRON DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE OINTMENT;OPHTHALMIC EQ 0.05% PHOSPHATE;EQ 3.5MG BASE/GM No No None 1969/09/15 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
1996/04/16 SUPPL-32(补充) Approval Manufacturing (CMC)
1995/11/20 SUPPL-12(补充) Approval Labeling
1995/11/20 SUPPL-11(补充) Approval Labeling
1995/11/20 SUPPL-9(补充) Approval Labeling
1995/11/20 SUPPL-8(补充) Approval Labeling
1995/06/12 SUPPL-31(补充) Approval Manufacturing (CMC)
1992/03/11 SUPPL-10(补充) Approval Manufacturing (CMC)
1987/12/15 SUPPL-7(补充) Approval Manufacturing (CMC)
1984/09/06 SUPPL-30(补充) Approval Manufacturing (CMC)
1984/09/06 SUPPL-4(补充) Approval Manufacturing (CMC)
1984/07/10 SUPPL-3(补充) Approval Labeling
1984/02/28 SUPPL-1(补充) Approval Manufacturing (CMC)
1982/07/20 SUPPL-29(补充) Approval Labeling
1981/10/13 SUPPL-28(补充) Approval Labeling
1981/09/29 SUPPL-27(补充) Approval Manufacturing (CMC)
1981/09/29 SUPPL-25(补充) Approval Manufacturing (CMC)
1981/01/13 SUPPL-24(补充) Approval Labeling
1980/08/28 SUPPL-23(补充) Approval Labeling
1980/04/01 SUPPL-22(补充) Approval Manufacturing (CMC)
1978/02/17 SUPPL-21(补充) Approval Manufacturing (CMC)
1978/01/27 SUPPL-20(补充) Approval Efficacy
1977/03/23 SUPPL-19(补充) Approval Labeling
1976/02/23 SUPPL-18(补充) Approval Manufacturing (CMC)
1976/01/09 SUPPL-17(补充) Approval Efficacy
1975/03/07 SUPPL-16(补充) Approval Manufacturing (CMC)
1973/12/18 SUPPL-15(补充) Approval Labeling
1972/09/07 SUPPL-14(补充) Approval Labeling
1972/08/31 SUPPL-13(补充) Approval Manufacturing (CMC)
1970/04/30 SUPPL-6(补充) Approval Labeling
1969/12/24 SUPPL-5(补充) Approval Manufacturing (CMC)
1969/11/03 SUPPL-2(补充) Approval Labeling
1969/09/15 ORIG-1(原始申请) Approval
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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