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=ANDA070976"
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
43353-316-09 43353-316 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20170503 N/A ANDA ANDA070976 Aphena Pharma Solutions - Tennessee, LLC CLONIDINE HYDROCHLORIDE .3 mg/1 9000 TABLET in 1 BOTTLE (43353-316-09)
0228-2129-10 0228-2129 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 19950103 N/A ANDA ANDA070976 Actavis Pharma, Inc. CLONIDINE HYDROCHLORIDE .3 mg/1 100 TABLET in 1 BOTTLE (0228-2129-10)
0615-2574-39 0615-2574 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20190207 N/A ANDA ANDA070976 NCS HealthCare of KY, LLC dba Vangard Labs CLONIDINE HYDROCHLORIDE .3 mg/1 30 TABLET in 1 BLISTER PACK (0615-2574-39)
67046-1005-3 67046-1005 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 20241111 N/A ANDA ANDA070976 Coupler LLC CLONIDINE HYDROCHLORIDE .3 mg/1 30 TABLET in 1 BLISTER PACK (67046-1005-3)
68001-239-00 68001-239 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET ORAL 19950103 N/A ANDA ANDA070976 BluePoint Laboratories CLONIDINE HYDROCHLORIDE .3 mg/1 100 TABLET in 1 BOTTLE (68001-239-00)
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