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
71335-2670-1	71335-2670	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250626	N/A	ANDA	ANDA074700	Bryant Ranch Prepack	BUMETANIDE	1 mg/1	500 TABLET in 1 BOTTLE (71335-2670-1)
0185-0128-01	0185-0128	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	19961121	N/A	ANDA	ANDA074700	Sandoz Inc	BUMETANIDE	.5 mg/1	100 TABLET in 1 BOTTLE (0185-0128-01)
0185-0128-05	0185-0128	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	19961121	N/A	ANDA	ANDA074700	Sandoz Inc	BUMETANIDE	.5 mg/1	500 TABLET in 1 BOTTLE (0185-0128-05)
50090-6308-0	50090-6308	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20221230	N/A	ANDA	ANDA074700	A-S Medication Solutions	BUMETANIDE	.5 mg/1	90 TABLET in 1 BOTTLE (50090-6308-0)
82804-119-90	82804-119	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20240708	N/A	ANDA	ANDA074700	Proficient Rx LP	BUMETANIDE	1 mg/1	90 TABLET in 1 BOTTLE (82804-119-90)
72162-2195-1	72162-2195	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20231215	N/A	ANDA	ANDA074700	Bryant Ranch Prepack	BUMETANIDE	.5 mg/1	100 TABLET in 1 BOTTLE (72162-2195-1)
0185-0129-01	0185-0129	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	19961121	N/A	ANDA	ANDA074700	Sandoz Inc	BUMETANIDE	1 mg/1	100 TABLET in 1 BOTTLE (0185-0129-01)
0185-0129-05	0185-0129	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	19961121	N/A	ANDA	ANDA074700	Sandoz Inc	BUMETANIDE	1 mg/1	500 TABLET in 1 BOTTLE (0185-0129-05)
70518-4387-0	70518-4387	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20250706	N/A	ANDA	ANDA074700	REMEDYREPACK INC.	BUMETANIDE	2 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4387-0)