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
82804-065-60 82804-065 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20240131 N/A ANDA ANDA202759 Proficient Rx LP GLIMEPIRIDE 2 mg/1 60 TABLET in 1 BOTTLE (82804-065-60)
82804-065-78 82804-065 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20260218 N/A ANDA ANDA202759 Proficient Rx LP GLIMEPIRIDE 2 mg/1 180 TABLET in 1 BOTTLE (82804-065-78)
82804-065-90 82804-065 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20240131 N/A ANDA ANDA202759 Proficient Rx LP GLIMEPIRIDE 2 mg/1 90 TABLET in 1 BOTTLE (82804-065-90)
82804-065-30 82804-065 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20240131 N/A ANDA ANDA202759 Proficient Rx LP GLIMEPIRIDE 2 mg/1 30 TABLET in 1 BOTTLE (82804-065-30)
65862-580-01 65862-580 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 2 mg/1 100 TABLET in 1 BOTTLE (65862-580-01)
65862-580-05 65862-580 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 2 mg/1 500 TABLET in 1 BOTTLE (65862-580-05)
65862-580-99 65862-580 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 2 mg/1 1000 TABLET in 1 BOTTLE (65862-580-99)
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)
65862-581-01 65862-581 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20120629 N/A ANDA ANDA202759 Aurobindo Pharma Limited GLIMEPIRIDE 4 mg/1 100 TABLET in 1 BOTTLE (65862-581-01)
82868-042-90 82868-042 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20240126 N/A ANDA ANDA202759 Northwind Health Company, LLC GLIMEPIRIDE 2 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (82868-042-90)
50090-6322-3 50090-6322 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230110 N/A ANDA ANDA202759 A-S Medication Solutions GLIMEPIRIDE 4 mg/1 90 TABLET in 1 BOTTLE (50090-6322-3)
50090-6322-4 50090-6322 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230110 N/A ANDA ANDA202759 A-S Medication Solutions GLIMEPIRIDE 4 mg/1 180 TABLET in 1 BOTTLE (50090-6322-4)
50090-6322-0 50090-6322 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230110 N/A ANDA ANDA202759 A-S Medication Solutions GLIMEPIRIDE 4 mg/1 30 TABLET in 1 BOTTLE (50090-6322-0)
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)
50090-6322-1 50090-6322 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230110 N/A ANDA ANDA202759 A-S Medication Solutions GLIMEPIRIDE 4 mg/1 100 TABLET in 1 BOTTLE (50090-6322-1)
50090-6322-2 50090-6322 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230110 N/A ANDA ANDA202759 A-S Medication Solutions GLIMEPIRIDE 4 mg/1 60 TABLET in 1 BOTTLE (50090-6322-2)
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