药品注册申请号:089271
申请类型:ANDA (仿制药申请)
申请人:MIKART
申请人全名:MIKART LLC
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 500MG;5MG No No None 1986/07/16 1986/07/16 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
2002/08/13 SUPPL-39(补充) Approval Manufacturing (CMC)
2000/08/31 SUPPL-33(补充) Approval Manufacturing (CMC)
2000/08/31 SUPPL-32(补充) Approval Manufacturing (CMC)
2000/08/31 SUPPL-31(补充) Approval Manufacturing (CMC)
2000/08/31 SUPPL-29(补充) Approval Manufacturing (CMC)
1998/09/09 SUPPL-38(补充) Approval Manufacturing (CMC)
1998/07/31 SUPPL-37(补充) Approval Manufacturing (CMC)
1998/01/14 SUPPL-36(补充) Approval Manufacturing (CMC)
1997/02/07 SUPPL-30(补充) Approval Labeling
1996/09/18 SUPPL-35(补充) Approval Manufacturing (CMC)
1996/09/18 SUPPL-34(补充) Approval Manufacturing (CMC)
1995/07/19 SUPPL-28(补充) Approval Manufacturing (CMC)
1995/02/08 SUPPL-27(补充) Approval Manufacturing (CMC)
1993/07/20 SUPPL-10(补充) Approval Manufacturing (CMC)
1993/07/20 SUPPL-9(补充) Approval Manufacturing (CMC)
1992/05/13 SUPPL-26(补充) Approval Manufacturing (CMC)
1992/01/06 SUPPL-25(补充) Approval Manufacturing (CMC)
1992/01/06 SUPPL-24(补充) Approval Manufacturing (CMC)
1992/01/06 SUPPL-23(补充) Approval Labeling
1992/01/06 SUPPL-22(补充) Approval Manufacturing (CMC)
1992/01/06 SUPPL-21(补充) Approval Labeling
1992/01/06 SUPPL-20(补充) Approval Manufacturing (CMC)
1991/02/21 SUPPL-19(补充) Approval Manufacturing (CMC)
1990/09/14 SUPPL-15(补充) Approval Manufacturing (CMC)
1990/09/14 SUPPL-14(补充) Approval Manufacturing (CMC)
1989/11/21 SUPPL-17(补充) Approval Labeling
1989/04/11 SUPPL-16(补充) Approval Bioequivalence
1989/03/02 SUPPL-13(补充) Approval Manufacturing (CMC)
1989/03/02 SUPPL-12(补充) Approval Manufacturing (CMC)
1989/03/02 SUPPL-11(补充) Approval Manufacturing (CMC)
1988/06/17 SUPPL-4(补充) Approval Manufacturing (CMC)
1988/05/12 SUPPL-1(补充) Approval Manufacturing (CMC)
1988/04/15 SUPPL-2(补充) Approval Manufacturing (CMC)
1986/07/16 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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