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=ANDA206069"
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
65862-806-05 65862-806 HUMAN PRESCRIPTION DRUG Armodafinil Armodafinil TABLET ORAL 20180306 N/A ANDA ANDA206069 Aurobindo Pharma Limited ARMODAFINIL 150 mg/1 500 TABLET in 1 BOTTLE (65862-806-05)
65862-806-30 65862-806 HUMAN PRESCRIPTION DRUG Armodafinil Armodafinil TABLET ORAL 20180306 N/A ANDA ANDA206069 Aurobindo Pharma Limited ARMODAFINIL 150 mg/1 30 TABLET in 1 BOTTLE (65862-806-30)
65862-806-60 65862-806 HUMAN PRESCRIPTION DRUG Armodafinil Armodafinil TABLET ORAL 20180306 N/A ANDA ANDA206069 Aurobindo Pharma Limited ARMODAFINIL 150 mg/1 60 TABLET in 1 BOTTLE (65862-806-60)
65862-807-05 65862-807 HUMAN PRESCRIPTION DRUG Armodafinil Armodafinil TABLET ORAL 20180306 N/A ANDA ANDA206069 Aurobindo Pharma Limited ARMODAFINIL 250 mg/1 500 TABLET in 1 BOTTLE (65862-807-05)
65862-807-30 65862-807 HUMAN PRESCRIPTION DRUG Armodafinil Armodafinil TABLET ORAL 20180306 N/A ANDA ANDA206069 Aurobindo Pharma Limited ARMODAFINIL 250 mg/1 30 TABLET in 1 BOTTLE (65862-807-30)
65862-807-60 65862-807 HUMAN PRESCRIPTION DRUG Armodafinil Armodafinil TABLET ORAL 20180306 N/A ANDA ANDA206069 Aurobindo Pharma Limited ARMODAFINIL 250 mg/1 60 TABLET in 1 BOTTLE (65862-807-60)
65862-998-30 65862-998 HUMAN PRESCRIPTION DRUG Armodafinil Armodafinil TABLET ORAL 20181207 N/A ANDA ANDA206069 Aurobindo Pharma Limited ARMODAFINIL 200 mg/1 30 TABLET in 1 BOTTLE (65862-998-30)
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