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=ANDA200831"
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
0591-3713-05 0591-3713 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20170612 N/A ANDA ANDA200831 Actavis Pharma, Inc. EZETIMIBE 10 mg/1 500 TABLET in 1 BOTTLE (0591-3713-05)
0591-3713-19 0591-3713 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20170612 N/A ANDA ANDA200831 Actavis Pharma, Inc. EZETIMIBE 10 mg/1 90 TABLET in 1 BOTTLE (0591-3713-19)
0591-3713-30 0591-3713 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20170612 N/A ANDA ANDA200831 Actavis Pharma, Inc. EZETIMIBE 10 mg/1 30 TABLET in 1 BOTTLE (0591-3713-30)
71335-0933-1 71335-0933 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20180823 N/A ANDA ANDA200831 Bryant Ranch Prepack EZETIMIBE 10 mg/1 30 TABLET in 1 BOTTLE (71335-0933-1)
71335-0933-2 71335-0933 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20180731 N/A ANDA ANDA200831 Bryant Ranch Prepack EZETIMIBE 10 mg/1 90 TABLET in 1 BOTTLE (71335-0933-2)
71335-0933-3 71335-0933 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20211228 N/A ANDA ANDA200831 Bryant Ranch Prepack EZETIMIBE 10 mg/1 28 TABLET in 1 BOTTLE (71335-0933-3)
71335-0933-4 71335-0933 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20211228 N/A ANDA ANDA200831 Bryant Ranch Prepack EZETIMIBE 10 mg/1 18 TABLET in 1 BOTTLE (71335-0933-4)
71335-0933-5 71335-0933 HUMAN PRESCRIPTION DRUG Ezetimibe Ezetimibe TABLET ORAL 20211228 N/A ANDA ANDA200831 Bryant Ranch Prepack EZETIMIBE 10 mg/1 60 TABLET in 1 BOTTLE (71335-0933-5)
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