美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA070975"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
70518-4357-0 70518-4357 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20250616 N/A ANDA ANDA070975 REMEDYREPACK INC. CLONIDINE HYDROCHLORIDE .2 mg/1 30 TABLET in 1 BLISTER PACK (70518-4357-0)
0228-2128-10 0228-2128 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 19950103 N/A ANDA ANDA070975 Actavis Pharma, Inc. CLONIDINE HYDROCHLORIDE .2 mg/1 100 TABLET in 1 BOTTLE (0228-2128-10)
0228-2128-50 0228-2128 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 19950103 N/A ANDA ANDA070975 Actavis Pharma, Inc. CLONIDINE HYDROCHLORIDE .2 mg/1 500 TABLET in 1 BOTTLE (0228-2128-50)
67046-0327-3 67046-0327 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20241107 N/A ANDA ANDA070975 Coupler LLC CLONIDINE HYDROCHLORIDE .2 mg/1 30 TABLET in 1 BLISTER PACK (67046-0327-3)
67046-1000-3 67046-1000 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20241108 N/A ANDA ANDA070975 Coupler LLC CLONIDINE HYDROCHLORIDE .2 mg/1 30 TABLET in 1 BLISTER PACK (67046-1000-3)
51655-362-26 51655-362 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20230721 N/A ANDA ANDA070975 Northwind Pharmaceuticals, LLC CLONIDINE HYDROCHLORIDE .2 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (51655-362-26)
51655-362-52 51655-362 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20140924 N/A ANDA ANDA070975 Northwind Pharmaceuticals, LLC CLONIDINE HYDROCHLORIDE .2 mg/1 30 TABLET in 1 BOTTLE, DISPENSING (51655-362-52)
68001-238-00 68001-238 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 19950103 N/A ANDA ANDA070975 BluePoint Laboratories CLONIDINE HYDROCHLORIDE .2 mg/1 100 TABLET in 1 BOTTLE (68001-238-00)
68001-238-03 68001-238 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 19950103 N/A ANDA ANDA070975 BluePoint Laboratories CLONIDINE HYDROCHLORIDE .2 mg/1 500 TABLET in 1 BOTTLE (68001-238-03)
60687-124-01 60687-124 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20200730 N/A ANDA ANDA070975 American Health Packaging CLONIDINE HYDROCHLORIDE .2 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-124-01) / 1 TABLET in 1 BLISTER PACK (60687-124-11)
55154-2577-0 55154-2577 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20200730 N/A ANDA ANDA070975 Cardinal Health 107, LLC CLONIDINE HYDROCHLORIDE .2 mg/1 10 BLISTER PACK in 1 BAG (55154-2577-0) / 1 TABLET in 1 BLISTER PACK
0615-8272-39 0615-8272 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20190306 N/A ANDA ANDA070975 NCS HealthCare of KY, LLC dba Vangard Labs CLONIDINE HYDROCHLORIDE .2 mg/1 30 TABLET in 1 BLISTER PACK (0615-8272-39)
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