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
72205-056-91	72205-056	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20260210	N/A	ANDA	ANDA215362	Novadoz Pharmaceuticals LLC	BUMETANIDE	.5 mg/1	100 TABLET in 1 BOTTLE (72205-056-91)
72205-057-05	72205-057	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20260210	N/A	ANDA	ANDA215362	Novadoz Pharmaceuticals LLC	BUMETANIDE	1 mg/1	500 TABLET in 1 BOTTLE (72205-057-05)
72205-057-91	72205-057	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20260210	N/A	ANDA	ANDA215362	Novadoz Pharmaceuticals LLC	BUMETANIDE	1 mg/1	100 TABLET in 1 BOTTLE (72205-057-91)
72205-058-05	72205-058	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20260210	N/A	ANDA	ANDA215362	Novadoz Pharmaceuticals LLC	BUMETANIDE	2 mg/1	500 TABLET in 1 BOTTLE (72205-058-05)
72205-058-91	72205-058	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20260210	N/A	ANDA	ANDA215362	Novadoz Pharmaceuticals LLC	BUMETANIDE	2 mg/1	100 TABLET in 1 BOTTLE (72205-058-91)