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=ANDA091220"
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
0615-8333-39 0615-8333 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20200413 N/A ANDA ANDA091220 NCS HealthCare of KY, Inc dba Vangard Labs GLIMEPIRIDE 2 mg/1 30 TABLET in 1 BLISTER PACK (0615-8333-39)
68001-586-00 68001-586 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230901 N/A ANDA ANDA091220 BluePoint Laboratories GLIMEPIRIDE 4 mg/1 100 TABLET in 1 BOTTLE (68001-586-00)
68001-586-03 68001-586 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230901 N/A ANDA ANDA091220 BluePoint Laboratories GLIMEPIRIDE 4 mg/1 500 TABLET in 1 BOTTLE (68001-586-03)
71335-1885-1 71335-1885 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20211109 N/A ANDA ANDA091220 Bryant Ranch Prepack GLIMEPIRIDE 1 mg/1 30 TABLET in 1 BOTTLE (71335-1885-1)
71335-1885-2 71335-1885 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20250616 N/A ANDA ANDA091220 Bryant Ranch Prepack GLIMEPIRIDE 1 mg/1 60 TABLET in 1 BOTTLE (71335-1885-2)
71335-1885-3 71335-1885 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20210528 N/A ANDA ANDA091220 Bryant Ranch Prepack GLIMEPIRIDE 1 mg/1 90 TABLET in 1 BOTTLE (71335-1885-3)
71335-1885-4 71335-1885 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20250616 N/A ANDA ANDA091220 Bryant Ranch Prepack GLIMEPIRIDE 1 mg/1 100 TABLET in 1 BOTTLE (71335-1885-4)
71335-1885-5 71335-1885 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20250616 N/A ANDA ANDA091220 Bryant Ranch Prepack GLIMEPIRIDE 1 mg/1 20 TABLET in 1 BOTTLE (71335-1885-5)
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