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=ANDA213942"
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
70518-4478-0 70518-4478 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250912 N/A ANDA ANDA213942 REMEDYREPACK INC. BUMETANIDE 2 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-4478-0)
72888-021-01 72888-021 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250116 N/A ANDA ANDA213942 Advagen Pharma Limited BUMETANIDE 2 mg/1 100 TABLET in 1 BOTTLE (72888-021-01)
72888-020-01 72888-020 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250116 N/A ANDA ANDA213942 Advagen Pharma Limited BUMETANIDE 1 mg/1 100 TABLET in 1 BOTTLE (72888-020-01)
72888-019-01 72888-019 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250116 N/A ANDA ANDA213942 Advagen Pharma Limited BUMETANIDE .5 mg/1 100 TABLET in 1 BOTTLE (72888-019-01)
70518-4385-0 70518-4385 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20250706 N/A ANDA ANDA213942 REMEDYREPACK INC. BUMETANIDE 1 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-4385-0)
50090-7736-0 50090-7736 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide TABLET ORAL 20251028 N/A ANDA ANDA213942 A-S Medication Solutions BUMETANIDE .5 mg/1 90 TABLET in 1 BOTTLE (50090-7736-0)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase