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
63629-4968-3	63629-4968	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20220429	N/A	ANDA	ANDA074700	Bryant Ranch Prepack	BUMETANIDE	1 mg/1	28 TABLET in 1 BOTTLE (63629-4968-3)
63629-4968-4	63629-4968	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20220429	N/A	ANDA	ANDA074700	Bryant Ranch Prepack	BUMETANIDE	1 mg/1	18 TABLET in 1 BOTTLE (63629-4968-4)
63629-4968-5	63629-4968	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20220429	N/A	ANDA	ANDA074700	Bryant Ranch Prepack	BUMETANIDE	1 mg/1	60 TABLET in 1 BOTTLE (63629-4968-5)
63629-4968-6	63629-4968	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20220429	N/A	ANDA	ANDA074700	Bryant Ranch Prepack	BUMETANIDE	1 mg/1	100 TABLET in 1 BOTTLE (63629-4968-6)
50090-6304-0	50090-6304	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20221229	N/A	ANDA	ANDA074700	A-S Medication Solutions	BUMETANIDE	2 mg/1	90 TABLET in 1 BOTTLE (50090-6304-0)
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)
71335-2998-1	71335-2998	HUMAN PRESCRIPTION DRUG	Bumetanide	Bumetanide	TABLET	ORAL	20251104	N/A	ANDA	ANDA074700	Bryant Ranch Prepack	BUMETANIDE	2 mg/1	100 TABLET in 1 BOTTLE (71335-2998-1)