药品注册申请号:018333
申请类型:NDA (新药申请)
申请人:ABBVIE
申请人全名:ABBVIE 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 CARAFATE SUCRALFATE TABLET;ORAL 1GM Yes Yes AB 1981/10/30 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
2013/03/04 SUPPL-34(补充) Approval Labeling STANDARD
2007/04/26 SUPPL-32(补充) Approval Labeling STANDARD
1995/11/29 SUPPL-29(补充) Approval Manufacturing (CMC) PRIORITY
1995/08/15 SUPPL-28(补充) Approval Manufacturing (CMC) PRIORITY
1994/07/14 SUPPL-27(补充) Approval Labeling STANDARD
1992/12/28 SUPPL-26(补充) Approval Labeling STANDARD
1991/02/12 SUPPL-25(补充) Approval Labeling
1990/10/05 SUPPL-24(补充) Approval Manufacturing (CMC) PRIORITY
1990/05/11 SUPPL-23(补充) Approval Labeling
1990/05/11 SUPPL-9(补充) Approval Efficacy
1988/12/19 SUPPL-17(补充) Approval Labeling
1988/12/16 SUPPL-22(补充) Approval Manufacturing (CMC) PRIORITY
1988/05/05 SUPPL-18(补充) Approval Manufacturing (CMC) PRIORITY
1987/08/05 SUPPL-12(补充) Approval Manufacturing (CMC) PRIORITY
1987/08/05 SUPPL-10(补充) Approval Manufacturing (CMC) PRIORITY
1986/07/02 SUPPL-14(补充) Approval Labeling
1985/09/24 SUPPL-11(补充) Approval Manufacturing (CMC) PRIORITY
1985/05/14 SUPPL-8(补充) Approval Labeling
1984/09/24 SUPPL-6(补充) Approval Labeling
1983/06/09 SUPPL-3(补充) Approval Manufacturing (CMC) PRIORITY
1983/06/01 SUPPL-4(补充) Approval Manufacturing (CMC) PRIORITY
1983/04/22 SUPPL-5(补充) Approval Labeling
1982/08/16 SUPPL-2(补充) Approval Labeling
1982/03/09 SUPPL-1(补充) Approval Manufacturing (CMC) PRIORITY
1981/10/30 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity PRIORITY
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号专利号专利过期日是否物质专利是否产品专利专利用途代码撤销请求提交日期专利下载备注
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
活性成分:SUCRALFATE 剂型/给药途径:TABLET;ORAL 规格:1GM 治疗等效代码:AB
申请号产品号申请类型商品名活性成分剂型/给药途径规格市场状态RLDRSTE Code产品号批准日期申请人
018333 001 NDA CARAFATE SUCRALFATE TABLET;ORAL 1GM Prescription Yes Yes AB Approved Prior to Jan 1, 1982 ABBVIE
070848 001 ANDA SUCRALFATE SUCRALFATE TABLET;ORAL 1GM Prescription No No AB 1996/03/29 TEVA
074415 001 ANDA SUCRALFATE SUCRALFATE TABLET;ORAL 1GM Prescription No No AB 1998/06/08 NOSTRUM LABS INC
215576 001 ANDA SUCRALFATE SUCRALFATE TABLET;ORAL 1GM Prescription No No AB 2022/04/15 AMNEAL PHARMS
215705 001 ANDA SUCRALFATE SUCRALFATE TABLET;ORAL 1GM Prescription No No AB 2023/05/03 ZYDUS LIFESCIENCES
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