药品注册申请号:017744
申请类型:NDA (新药申请)
申请人:SEBELA IRELAND LTD
申请人全名:SEBELA IRELAND LTD
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 MOTOFEN HALF-STRENGTH ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE TABLET;ORAL 0.025MG;0.5MG No No None 1978/07/14 Approved Prior to Jan 1, 1982 Discontinued
002 MOTOFEN ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE TABLET;ORAL 0.025MG;1MG Yes Yes None Approved Prior to Jan 1, 1982 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
2017/03/28 SUPPL-26(补充) Approval Labeling STANDARD
2001/12/17 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
2001/08/17 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
2001/05/25 SUPPL-21(补充) Approval Manufacturing (CMC) STANDARD
1999/09/03 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1999/01/07 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1999/01/07 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1998/10/08 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1997/08/13 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1997/01/27 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1996/08/29 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1996/08/29 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1996/08/29 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1996/08/19 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1992/04/29 SUPPL-10(补充) Approval Labeling
1991/12/03 SUPPL-5(补充) Approval Labeling
1991/01/29 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1988/08/19 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1988/07/20 SUPPL-3(补充) Approval Labeling
1982/04/21 SUPPL-2(补充) Approval Labeling
1981/12/28 SUPPL-1(补充) Approval Labeling
1978/07/14 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity and Type 4 - New Combination 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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