药品注册申请号:019992
申请类型:NDA (新药申请)
申请人:SANDOZ
申请人全名:SANDOZ 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 CILOXAN CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Yes Yes AT 1990/12/31 1990/12/31 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
2017/03/21 SUPPL-26(补充) Approval Labeling STANDARD
2006/02/07 SUPPL-20(补充) Approval Labeling STANDARD
2004/08/20 SUPPL-19(补充) Approval Labeling STANDARD
2002/03/13 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
2001/09/14 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
2001/03/16 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
2000/02/18 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1999/11/09 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1999/08/17 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1999/03/11 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1999/02/05 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1998/10/14 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1998/01/15 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1995/11/01 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1995/11/01 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1994/10/27 SUPPL-4(补充) Approval Efficacy STANDARD
1993/10/27 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1993/01/22 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1992/02/12 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1990/12/31 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:CIPROFLOXACIN HYDROCHLORIDE 剂型/给药途径:SOLUTION/DROPS;OPHTHALMIC 规格:EQ 0.3% BASE 治疗等效代码:AT
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
019992 001 NDA CILOXAN CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Prescription Yes Yes AT 1990/12/31 SANDOZ
075928 001 ANDA CIPROFLOXACIN HYDROCHLORIDE CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Prescription No No AT 2004/06/09 RUBICON
076754 001 ANDA CIPROFLOXACIN HYDROCHLORIDE CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Discontinued No No AT 2004/06/09 PAI HOLDINGS PHARM
076673 001 ANDA CIPROFLOXACIN HYDROCHLORIDE CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Prescription No No AT 2005/01/21 WATSON LABS INC
077689 001 ANDA CIPROFLOXACIN HYDROCHLORIDE CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Prescription No No AT 2006/12/13 RISING
077568 001 ANDA CIPROFLOXACIN HYDROCHLORIDE CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Prescription No No AT 2008/06/30 FDC LTD
076555 001 ANDA CIPROFLOXACIN HYDROCHLORIDE CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Discontinued No No AT 2008/12/11 SAPTALIS PHARMS
204613 001 ANDA CIPROFLOXACIN HYDROCHLORIDE CIPROFLOXACIN HYDROCHLORIDE SOLUTION/DROPS;OPHTHALMIC EQ 0.3% BASE Prescription No No AT 2018/05/03 ALTAIRE PHARMS INC
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