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=ANDA202112"
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
50090-7406-2 50090-7406 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20241024 N/A ANDA ANDA202112 A-S Medication Solutions GLIMEPIRIDE 4 mg/1 60 TABLET in 1 BOTTLE (50090-7406-2)
50090-7406-3 50090-7406 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20241024 N/A ANDA ANDA202112 A-S Medication Solutions GLIMEPIRIDE 4 mg/1 90 TABLET in 1 BOTTLE (50090-7406-3)
71335-9657-1 71335-9657 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230227 N/A ANDA ANDA202112 Bryant Ranch Prepack GLIMEPIRIDE 2 mg/1 30 TABLET in 1 BOTTLE (71335-9657-1)
71335-9657-5 71335-9657 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230227 N/A ANDA ANDA202112 Bryant Ranch Prepack GLIMEPIRIDE 2 mg/1 180 TABLET in 1 BOTTLE (71335-9657-5)
71335-9657-2 71335-9657 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230227 N/A ANDA ANDA202112 Bryant Ranch Prepack GLIMEPIRIDE 2 mg/1 60 TABLET in 1 BOTTLE (71335-9657-2)
71335-9657-3 71335-9657 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230227 N/A ANDA ANDA202112 Bryant Ranch Prepack GLIMEPIRIDE 2 mg/1 90 TABLET in 1 BOTTLE (71335-9657-3)
71335-9657-4 71335-9657 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230227 N/A ANDA ANDA202112 Bryant Ranch Prepack GLIMEPIRIDE 2 mg/1 100 TABLET in 1 BOTTLE (71335-9657-4)
71921-214-01 71921-214 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230731 N/A ANDA ANDA202112 Florida Pharmaceutical Products, LLC GLIMEPIRIDE 1 mg/1 100 TABLET in 1 BOTTLE (71921-214-01)
71921-216-01 71921-216 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230731 N/A ANDA ANDA202112 Florida Pharmaceutical Products, LLC GLIMEPIRIDE 4 mg/1 100 TABLET in 1 BOTTLE (71921-216-01)
71921-216-50 71921-216 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230731 N/A ANDA ANDA202112 Florida Pharmaceutical Products, LLC GLIMEPIRIDE 4 mg/1 500 TABLET in 1 BOTTLE (71921-216-50)
71921-214-50 71921-214 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230731 N/A ANDA ANDA202112 Florida Pharmaceutical Products, LLC GLIMEPIRIDE 1 mg/1 500 TABLET in 1 BOTTLE (71921-214-50)
71921-215-01 71921-215 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230731 N/A ANDA ANDA202112 Florida Pharmaceutical Products, LLC GLIMEPIRIDE 2 mg/1 100 TABLET in 1 BOTTLE (71921-215-01)
71921-215-50 71921-215 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230731 N/A ANDA ANDA202112 Florida Pharmaceutical Products, LLC GLIMEPIRIDE 2 mg/1 500 TABLET in 1 BOTTLE (71921-215-50)
72189-453-90 72189-453 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20230324 N/A ANDA ANDA202112 Direct_Rx GLIMEPIRIDE 4 mg/1 90 TABLET in 1 BOTTLE (72189-453-90)
72189-585-90 72189-585 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20240926 N/A ANDA ANDA202112 Direct_rx GLIMEPIRIDE 4 mg/1 90 TABLET in 1 BOTTLE (72189-585-90)
67046-1608-3 67046-1608 HUMAN PRESCRIPTION DRUG Glimepiride Glimepiride TABLET ORAL 20251022 N/A ANDA ANDA202112 Coupler LLC GLIMEPIRIDE 2 mg/1 30 TABLET in 1 BLISTER PACK (67046-1608-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase