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
0832-0541-10	0832-0541	HUMAN PRESCRIPTION DRUG	Bumetanide	BUMETANIDE	TABLET	ORAL	20180130	20260930	ANDA	ANDA209916	Upsher-Smith Laboratories, LLC	BUMETANIDE	1 mg/1	1000 TABLET in 1 BOTTLE (0832-0541-10)
0832-0541-11	0832-0541	HUMAN PRESCRIPTION DRUG	Bumetanide	BUMETANIDE	TABLET	ORAL	20180130	20260930	ANDA	ANDA209916	Upsher-Smith Laboratories, LLC	BUMETANIDE	1 mg/1	100 TABLET in 1 BOTTLE (0832-0541-11)
0832-0540-11	0832-0540	HUMAN PRESCRIPTION DRUG	Bumetanide	BUMETANIDE	TABLET	ORAL	20180130	20260630	ANDA	ANDA209916	Upsher-Smith Laboratories, LLC	BUMETANIDE	.5 mg/1	100 TABLET in 1 BOTTLE (0832-0540-11)
50090-7350-0	50090-7350	HUMAN PRESCRIPTION DRUG	Bumetanide	BUMETANIDE	TABLET	ORAL	20241016	N/A	ANDA	ANDA209916	A-S Medication Solutions	BUMETANIDE	2 mg/1	90 TABLET in 1 BOTTLE (50090-7350-0)
0832-0542-10	0832-0542	HUMAN PRESCRIPTION DRUG	Bumetanide	BUMETANIDE	TABLET	ORAL	20180130	20260930	ANDA	ANDA209916	Upsher-Smith Laboratories, LLC	BUMETANIDE	2 mg/1	1000 TABLET in 1 BOTTLE (0832-0542-10)
0832-0542-11	0832-0542	HUMAN PRESCRIPTION DRUG	Bumetanide	BUMETANIDE	TABLET	ORAL	20180130	20260930	ANDA	ANDA209916	Upsher-Smith Laboratories, LLC	BUMETANIDE	2 mg/1	100 TABLET in 1 BOTTLE (0832-0542-11)