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=ANDA202900"
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
68382-527-01 68382-527 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Pharmaceuticals (USA) Inc. BUMETANIDE 2 mg/1 100 TABLET in 1 BOTTLE (68382-527-01)
68382-527-05 68382-527 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Pharmaceuticals (USA) Inc. BUMETANIDE 2 mg/1 500 TABLET in 1 BOTTLE (68382-527-05)
68382-527-06 68382-527 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Pharmaceuticals (USA) Inc. BUMETANIDE 2 mg/1 30 TABLET in 1 BOTTLE (68382-527-06)
68382-527-10 68382-527 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Pharmaceuticals (USA) Inc. BUMETANIDE 2 mg/1 1000 TABLET in 1 BOTTLE (68382-527-10)
68382-527-16 68382-527 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Pharmaceuticals (USA) Inc. BUMETANIDE 2 mg/1 90 TABLET in 1 BOTTLE (68382-527-16)
50090-6138-2 50090-6138 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20221003 N/A ANDA ANDA202900 A-S Medication Solutions BUMETANIDE 1 mg/1 90 TABLET in 1 BOTTLE (50090-6138-2)
70771-1026-0 70771-1026 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Lifesciences Limited BUMETANIDE 2 mg/1 1000 TABLET in 1 BOTTLE (70771-1026-0)
70771-1026-1 70771-1026 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Lifesciences Limited BUMETANIDE 2 mg/1 100 TABLET in 1 BOTTLE (70771-1026-1)
70771-1026-3 70771-1026 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Lifesciences Limited BUMETANIDE 2 mg/1 30 TABLET in 1 BOTTLE (70771-1026-3)
70771-1026-5 70771-1026 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Lifesciences Limited BUMETANIDE 2 mg/1 500 TABLET in 1 BOTTLE (70771-1026-5)
70771-1026-9 70771-1026 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20180501 N/A ANDA ANDA202900 Zydus Lifesciences Limited BUMETANIDE 2 mg/1 90 TABLET in 1 BOTTLE (70771-1026-9)
71335-1692-1 71335-1692 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20200817 N/A ANDA ANDA202900 Bryant Ranch Prepack BUMETANIDE 1 mg/1 30 TABLET in 1 BOTTLE (71335-1692-1)
71335-1692-2 71335-1692 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20211229 N/A ANDA ANDA202900 Bryant Ranch Prepack BUMETANIDE 1 mg/1 90 TABLET in 1 BOTTLE (71335-1692-2)
71335-1692-3 71335-1692 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20211229 N/A ANDA ANDA202900 Bryant Ranch Prepack BUMETANIDE 1 mg/1 28 TABLET in 1 BOTTLE (71335-1692-3)
71335-1692-4 71335-1692 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20211229 N/A ANDA ANDA202900 Bryant Ranch Prepack BUMETANIDE 1 mg/1 18 TABLET in 1 BOTTLE (71335-1692-4)
71335-1692-5 71335-1692 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20211229 N/A ANDA ANDA202900 Bryant Ranch Prepack BUMETANIDE 1 mg/1 60 TABLET in 1 BOTTLE (71335-1692-5)
71335-1692-6 71335-1692 HUMAN PRESCRIPTION DRUG bumetanide bumetanide TABLET ORAL 20211229 N/A ANDA ANDA202900 Bryant Ranch Prepack BUMETANIDE 1 mg/1 100 TABLET in 1 BOTTLE (71335-1692-6)
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