药品注册申请号：216420
申请类型：ANDA (仿制药申请)
申请人：MICRO LABS
申请人全名：MICRO LABS LTD
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 NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) No No AP 2023/07/07 2023/07/07 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
2023/07/07 ORIG-1（原始申请） Approval 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
无
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
无
与本品治疗等效的药品
活性成分:NICARDIPINE HYDROCHLORIDE 剂型/给药途径:INJECTABLE;INJECTION 规格:25MG/10ML (2.5MG/ML) 治疗等效代码:AP
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
022276 001 NDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Prescription Yes Yes AP 2008/07/24 HIKMA INTL PHARMS
078405 001 NDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Discontinued No No AP 2009/11/17 SUN PHARM
090534 001 ANDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Prescription No Yes AP 2009/11/17 AM REGENT
090664 001 ANDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Prescription No No AP 2009/11/17 RK PHARMA
090671 001 ANDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Prescription No No AP 2009/11/17 WOCKHARDT
211121 001 ANDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Prescription No No AP 2021/04/08 EUGIA PHARMA
216420 001 ANDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Prescription No No AP 2023/07/07 MICRO LABS
217548 001 ANDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Prescription No No AP 2024/09/06 CHENGDU SHUODE
215406 001 ANDA NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE INJECTABLE;INJECTION 25MG/10ML (2.5MG/ML) Prescription No No AP 2024/10/31 AMNEAL
更多信息
药品NDC数据与药品包装、标签说明书
参考引用1
参考引用2
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