药品注册申请号:050720
申请类型:NDA (新药申请)
申请人:US ANTIBIOTICS
申请人全名:US ANTIBIOTICS 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 AUGMENTIN '875' AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Yes No AB 1996/02/13 1996/02/13 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
2024/05/01 SUPPL-37(补充) Approval Labeling STANDARD
2022/08/25 SUPPL-33(补充) Approval Labeling STANDARD
2014/09/30 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
2014/03/28 SUPPL-30(补充) Approval Manufacturing (CMC) STANDARD
2013/01/22 SUPPL-28(补充) Approval Labeling STANDARD Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs.
2013/01/22 SUPPL-26(补充) Approval Labeling STANDARD
2011/09/29 SUPPL-25(补充) Approval Labeling STANDARD
2008/12/04 SUPPL-23(补充) Approval Labeling STANDARD
2008/06/09 SUPPL-22(补充) Approval Labeling STANDARD
2008/04/07 SUPPL-24(补充) Approval Labeling STANDARD
2005/08/05 SUPPL-21(补充) Approval Labeling STANDARD
2004/08/30 SUPPL-19(补充) Approval Labeling STANDARD
2004/05/27 SUPPL-18(补充) Approval Labeling STANDARD
2003/07/25 SUPPL-15(补充) Approval Labeling STANDARD
2002/12/04 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
2002/10/17 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
2002/05/01 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
2002/04/10 SUPPL-6(补充) Approval Labeling STANDARD
2001/05/03 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
2001/04/17 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1999/11/19 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1999/09/23 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1999/02/01 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1998/02/11 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1998/02/11 SUPPL-3(补充) Approval Labeling STANDARD
1997/10/20 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1997/03/19 SUPPL-2(补充) Approval Labeling STANDARD
1996/05/15 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1996/02/13 ORIG-1(原始申请) Approval Type 3 - New Dosage Form STANDARD
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:AMOXICILLIN; CLAVULANATE POTASSIUM 剂型/给药途径:TABLET;ORAL 规格:875MG;EQ 125MG BASE 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
050720 001 NDA AUGMENTIN '875' AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Prescription Yes No AB 1996/02/13 US ANTIBIOTICS
065063 001 ANDA AMOXICILLIN AND CLAVULANATE POTASSIUM AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Prescription No Yes AB 2002/03/14 SANDOZ
065096 001 ANDA AMOXICILLIN AND CLAVULANATE POTASSIUM AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Prescription No No AB 2002/10/29 TEVA PHARMS USA
065093 001 ANDA AMOXICILLIN AND CLAVULANATE POTASSIUM AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Prescription No No AB 2002/11/21 SANDOZ INC
091568 001 ANDA AMOXICILLIN AND CLAVULANATE POTASSIUM AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Prescription No No AB 2012/01/20 AUROBINDO PHARMA LTD
203824 001 ANDA AMOXICILLIN AND CLAVULANATE POTASSIUM AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Prescription No No AB 2016/08/23 HIKMA PHARMS
204755 003 ANDA AMOXICILLIN AND CLAVULANATE POTASSIUM AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Prescription No No AB 2016/12/30 MICRO LABS LTD INDIA
209991 001 ANDA AMOXICILLIN AND CLAVULANATE POTASSIUM AMOXICILLIN; CLAVULANATE POTASSIUM TABLET;ORAL 875MG;EQ 125MG BASE Prescription No No AB 2023/09/15 DEVA HOLDING AS
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