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=ANDA202759"
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
65862-581-05 65862-581 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 4 mg/1 500 TABLET in 1 BOTTLE (65862-581-05)
65862-581-25 65862-581 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 4 mg/1 250 TABLET in 1 BOTTLE (65862-581-25)
65862-581-99 65862-581 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 4 mg/1 1000 TABLET in 1 BOTTLE (65862-581-99)
65862-579-01 65862-579 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 1 mg/1 100 TABLET in 1 BOTTLE (65862-579-01)
65862-579-05 65862-579 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 1 mg/1 500 TABLET in 1 BOTTLE (65862-579-05)
65862-579-99 65862-579 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 1 mg/1 1000 TABLET in 1 BOTTLE (65862-579-99)
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