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=ANDA209757"
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
43547-435-06 43547-435 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20180215 N/A ANDA ANDA209757 Solco Healthcare LLC CLONIDINE HYDROCHLORIDE .1 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (43547-435-06)
71034-001-60 71034-001 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20171201 N/A ANDA ANDA209757 Xiamen LP Pharmaceutical Co., Ltd. CLONIDINE HYDROCHLORIDE .1 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71034-001-60)
72162-1367-6 72162-1367 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240716 N/A ANDA ANDA209757 Bryant Ranch Prepack CLONIDINE HYDROCHLORIDE .1 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1367-6)
63629-1208-1 63629-1208 HUMAN PRESCRIPTION DRUG Clonidine Hydrochloride Clonidine Hydrochloride TABLET, EXTENDED RELEASE ORAL 20240708 N/A ANDA ANDA209757 Bryant Ranch Prepack CLONIDINE HYDROCHLORIDE .1 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1208-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase