药品注册申请号:071655
申请类型:ANDA (仿制药申请)
申请人:TEVA PHARMS USA
申请人全名:TEVA PHARMACEUTICALS USA 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 OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG No No AB 1988/11/14 1988/11/14 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
2012/06/13 SUPPL-25(补充) Approval Labeling STANDARD
2011/10/28 SUPPL-24(补充) Approval Labeling
2010/03/09 SUPPL-23(补充) Approval Labeling
2008/02/19 SUPPL-15(补充) Approval Labeling
2001/05/29 SUPPL-12(补充) Approval Manufacturing (CMC)
2001/05/24 SUPPL-10(补充) Approval Manufacturing (CMC)
2001/05/24 SUPPL-9(补充) Approval Manufacturing (CMC)
2001/05/24 SUPPL-8(补充) Approval Manufacturing (CMC)
2001/03/20 SUPPL-11(补充) Approval Manufacturing (CMC)
2000/07/07 SUPPL-7(补充) Approval Manufacturing (CMC)
1996/10/31 SUPPL-6(补充) Approval Manufacturing (CMC)
1994/05/11 SUPPL-5(补充) Approval Manufacturing (CMC)
1994/02/15 SUPPL-1(补充) Approval Manufacturing (CMC)
1992/06/04 SUPPL-4(补充) Approval Labeling
1992/02/27 SUPPL-3(补充) Approval Labeling
1990/02/21 SUPPL-2(补充) Approval Labeling
1988/11/14 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)
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:OXYBUTYNIN CHLORIDE 剂型/给药途径:TABLET;ORAL 规格:5MG 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
071655 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 1988/11/14 TEVA PHARMS USA
074625 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 1996/07/31 UPSHER SMITH LABS
075079 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No Yes AB 1997/10/31 STRIDES PHARMA
209823 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 2017/10/23 NOVITIUM PHARMA
209025 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 2017/12/21 RISING
209335 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 2017/12/22 ABHAI LLC
210125 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 2018/09/06 TULEX PHARMS INC
211682 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Discontinued No No AB 2019/05/10 AVET LIFESCIENCES
210611 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 2019/10/30 NOVAST LABS
212798 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 2020/04/06 LEADING
208165 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 2020/12/17 STRIDES PHARMA
213550 001 ANDA OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE TABLET;ORAL 5MG Prescription No No AB 2022/07/14 BEXIMCO PHARMS USA
更多信息
药品NDC数据与药品包装、标签说明书
©2006-2024 DrugFuture->U.S. FDA Drugs Database