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）

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
76282-799-01	76282-799	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Exelan Pharmaceuticals, Inc.	BUMETANIDE	2 mg/1	100 TABLET in 1 BOTTLE (76282-799-01)
76282-799-05	76282-799	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Exelan Pharmaceuticals, Inc.	BUMETANIDE	2 mg/1	500 TABLET in 1 BOTTLE (76282-799-05)
76282-798-05	76282-798	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Exelan Pharmaceuticals, Inc.	BUMETANIDE	1 mg/1	500 TABLET in 1 BOTTLE (76282-798-05)
43547-897-50	43547-897	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Solco Healthcare LLC	BUMETANIDE	1 mg/1	500 TABLET in 1 BOTTLE (43547-897-50)
76282-798-01	76282-798	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Exelan Pharmaceuticals, Inc.	BUMETANIDE	1 mg/1	100 TABLET in 1 BOTTLE (76282-798-01)
43547-898-10	43547-898	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Solco Healthcare LLC	BUMETANIDE	2 mg/1	100 TABLET in 1 BOTTLE (43547-898-10)
43547-898-50	43547-898	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Solco Healthcare LLC	BUMETANIDE	2 mg/1	500 TABLET in 1 BOTTLE (43547-898-50)
76282-797-01	76282-797	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Exelan Pharmaceuticals, Inc.	BUMETANIDE	.5 mg/1	100 TABLET in 1 BOTTLE (76282-797-01)
43547-896-10	43547-896	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Solco Healthcare LLC	BUMETANIDE	.5 mg/1	100 TABLET in 1 BOTTLE (43547-896-10)
43547-897-10	43547-897	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250301	N/A	ANDA	ANDA212931	Solco Healthcare LLC	BUMETANIDE	1 mg/1	100 TABLET in 1 BOTTLE (43547-897-10)