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
42799-119-01	42799-119	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20151015	N/A	NDA AUTHORIZED GENERIC	NDA018225	Edenbridge Pharmaceuticals LLC.	BUMETANIDE	.5 mg/1	100 TABLET in 1 BOTTLE (42799-119-01)
42799-120-01	42799-120	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20151015	N/A	NDA AUTHORIZED GENERIC	NDA018225	Edenbridge Pharmaceuticals LLC.	BUMETANIDE	1 mg/1	100 TABLET in 1 BOTTLE (42799-120-01)
42799-120-02	42799-120	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20151015	N/A	NDA AUTHORIZED GENERIC	NDA018225	Edenbridge Pharmaceuticals LLC.	BUMETANIDE	1 mg/1	500 TABLET in 1 BOTTLE (42799-120-02)
42799-121-01	42799-121	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20151015	N/A	NDA AUTHORIZED GENERIC	NDA018225	Edenbridge Pharmaceuticals LLC.	BUMETANIDE	2 mg/1	100 TABLET in 1 BOTTLE (42799-121-01)
42799-121-02	42799-121	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20151015	N/A	NDA AUTHORIZED GENERIC	NDA018225	Edenbridge Pharmaceuticals LLC.	BUMETANIDE	2 mg/1	500 TABLET in 1 BOTTLE (42799-121-02)
60687-384-25	60687-384	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20180802	N/A	NDA AUTHORIZED GENERIC	NDA018225	American Health Packaging	BUMETANIDE	1 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-25) / 1 TABLET in 1 BLISTER PACK (60687-384-95)
60687-384-65	60687-384	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20230601	N/A	NDA AUTHORIZED GENERIC	NDA018225	American Health Packaging	BUMETANIDE	1 mg/1	50 BLISTER PACK in 1 CARTON (60687-384-65) / 1 TABLET in 1 BLISTER PACK (60687-384-11)
60687-384-01	60687-384	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20200713	N/A	NDA AUTHORIZED GENERIC	NDA018225	American Health Packaging	BUMETANIDE	1 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-01) / 1 TABLET in 1 BLISTER PACK (60687-384-11)
60687-535-01	60687-535	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20200713	N/A	NDA AUTHORIZED GENERIC	NDA018225	American Health Packaging	BUMETANIDE	2 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-535-01) / 1 TABLET in 1 BLISTER PACK (60687-535-11)
30698-630-01	30698-630	HUMAN PRESCRIPTION DRUG	Bumex	Bumetanide	TABLET	ORAL	19830228	N/A	NDA	NDA018225	Validus Pharmaceuticals LLC	BUMETANIDE	.5 mg/1	100 TABLET in 1 BOTTLE (30698-630-01)
30698-631-01	30698-631	HUMAN PRESCRIPTION DRUG	Bumex	Bumetanide	TABLET	ORAL	19830228	N/A	NDA	NDA018225	Validus Pharmaceuticals LLC	BUMETANIDE	1 mg/1	100 TABLET in 1 BOTTLE (30698-631-01)
30698-632-01	30698-632	HUMAN PRESCRIPTION DRUG	Bumex	Bumetanide	TABLET	ORAL	19830228	N/A	NDA	NDA018225	Validus Pharmaceuticals LLC	BUMETANIDE	2 mg/1	100 TABLET in 1 BOTTLE (30698-632-01)
50090-5064-0	50090-5064	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20200528	N/A	NDA AUTHORIZED GENERIC	NDA018225	A-S Medication Solutions	BUMETANIDE	2 mg/1	90 TABLET in 1 BOTTLE (50090-5064-0)
50090-5068-2	50090-5068	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20200529	N/A	NDA AUTHORIZED GENERIC	NDA018225	A-S Medication Solutions	BUMETANIDE	1 mg/1	90 TABLET in 1 BOTTLE (50090-5068-2)