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=ANDA207311"
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
60429-982-05 60429-982 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20171106 N/A ANDA ANDA207311 Golden State Medical Supply, Inc. EZETIMIBE 10 mg/1 500 TABLET in 1 BOTTLE (60429-982-05)
60429-982-30 60429-982 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20171106 N/A ANDA ANDA207311 Golden State Medical Supply, Inc. EZETIMIBE 10 mg/1 30 TABLET in 1 BOTTLE (60429-982-30)
60429-982-90 60429-982 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20171106 N/A ANDA ANDA207311 Golden State Medical Supply, Inc. EZETIMIBE 10 mg/1 90 TABLET in 1 BOTTLE (60429-982-90)
51660-200-90 51660-200 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20170612 N/A ANDA ANDA207311 Ohm Laboratories Inc. EZETIMIBE 10 mg/1 90 TABLET in 1 BOTTLE (51660-200-90)
51660-200-30 51660-200 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20170612 N/A ANDA ANDA207311 Ohm Laboratories Inc. EZETIMIBE 10 mg/1 30 TABLET in 1 BOTTLE (51660-200-30)
51660-200-05 51660-200 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20170612 N/A ANDA ANDA207311 Ohm Laboratories Inc. EZETIMIBE 10 mg/1 500 TABLET in 1 BOTTLE (51660-200-05)
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