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=ANDA078560"
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
68462-226-30 68462-226 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20220429 N/A ANDA ANDA078560 Glenmark Pharmaceuticals Inc., USA EZETIMIBE 10 mg/1 30 TABLET in 1 BOTTLE (68462-226-30)
68462-226-90 68462-226 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20220429 N/A ANDA ANDA078560 Glenmark Pharmaceuticals Inc., USA EZETIMIBE 10 mg/1 90 TABLET in 1 BOTTLE (68462-226-90)
68462-226-11 68462-226 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20220429 N/A ANDA ANDA078560 Glenmark Pharmaceuticals Inc., USA EZETIMIBE 10 mg/1 10 BLISTER PACK in 1 CARTON (68462-226-11) / 10 TABLET in 1 BLISTER PACK
68462-226-10 68462-226 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20220429 N/A ANDA ANDA078560 Glenmark Pharmaceuticals Inc., USA EZETIMIBE 10 mg/1 1000 TABLET in 1 BOTTLE (68462-226-10)
68462-226-05 68462-226 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20220429 N/A ANDA ANDA078560 Glenmark Pharmaceuticals Inc., USA EZETIMIBE 10 mg/1 500 TABLET in 1 BOTTLE (68462-226-05)
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