药品注册申请号:040084
申请类型:ANDA (仿制药申请)
申请人:MALLINCKRODT
申请人全名:MALLINCKRODT CHEMICAL 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 HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHEN; HYDROCODONE BITARTRATE TABLET;ORAL 750MG;7.5MG No No None 1995/06/01 1995/06/01 Discontinued
002 HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHEN; HYDROCODONE BITARTRATE TABLET;ORAL 500MG;5MG No No None 1995/06/01 Discontinued
003 HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHEN; HYDROCODONE BITARTRATE TABLET;ORAL 660MG;10MG No No None 1996/07/29 Discontinued
004 HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHEN; HYDROCODONE BITARTRATE TABLET;ORAL 650MG;10MG No No None 1996/10/16 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
2011/06/24 SUPPL-40(补充) Approval Labeling
2004/12/24 SUPPL-28(补充) Approval Supplement
2004/12/16 SUPPL-26(补充) Approval Supplement
2004/12/16 SUPPL-25(补充) Approval Supplement
2004/06/01 SUPPL-24(补充) Approval Supplement
2003/11/13 SUPPL-23(补充) Approval Supplement
2003/07/16 SUPPL-22(补充) Approval Supplement
2003/04/25 SUPPL-21(补充) Approval Supplement
2003/04/10 SUPPL-20(补充) Approval Supplement
2002/12/02 SUPPL-18(补充) Approval Labeling
2002/12/02 SUPPL-17(补充) Approval Manufacturing (CMC)
2002/09/27 SUPPL-19(补充) Approval Manufacturing (CMC)
2002/04/11 SUPPL-16(补充) Approval Manufacturing (CMC)
2000/03/13 SUPPL-15(补充) Approval Labeling
2000/03/13 SUPPL-14(补充) Approval Manufacturing (CMC)
2000/03/13 SUPPL-13(补充) Approval Manufacturing (CMC)
2000/03/13 SUPPL-12(补充) Approval Manufacturing (CMC)
2000/03/13 SUPPL-11(补充) Approval Manufacturing (CMC)
2000/03/13 SUPPL-10(补充) Approval Manufacturing (CMC)
1997/07/11 SUPPL-9(补充) Approval Labeling
1996/10/16 SUPPL-8(补充) Approval Labeling
1996/10/16 SUPPL-7(补充) Approval Manufacturing (CMC)
1996/07/29 SUPPL-2(补充) Approval Labeling
1996/07/29 SUPPL-1(补充) Approval Manufacturing (CMC)
1996/07/03 SUPPL-6(补充) Approval Labeling
1996/07/03 SUPPL-5(补充) Approval Manufacturing (CMC)
1996/07/03 SUPPL-4(补充) Approval Labeling
1996/07/03 SUPPL-3(补充) Approval Manufacturing (CMC)
1995/06/01 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
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与本品治疗等效的药品
本品无治疗等效药品
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