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
68382-661-01	68382-661	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-661-01)
68382-661-05	68382-661	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-661-05)
68382-661-06	68382-661	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-661-06)
68382-661-10	68382-661	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-661-10)
68382-661-16	68382-661	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-661-16)
68382-661-30	68382-661	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	50 mg/1	10 BLISTER PACK in 1 CARTON (68382-661-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
0904-6927-61	0904-6927	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Major Pharmaceuticals	SPIRONOLACTONE	25 mg/1	100 BLISTER PACK in 1 CARTON (0904-6927-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
60687-476-01	60687-476	HUMAN PRESCRIPTION DRUG	Spironolactone	Spironolactone	TABLET	ORAL	20190606	N/A	ANDA	ANDA205936	American Health Packaging	SPIRONOLACTONE	50 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-476-01) / 1 TABLET in 1 BLISTER PACK (60687-476-11)
55154-3556-0	55154-3556	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Cardinal Health 107, LLC	SPIRONOLACTONE	25 mg/1	10 BLISTER PACK in 1 BAG (55154-3556-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
68382-662-01	68382-662	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-662-01)
68382-662-05	68382-662	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-662-05)
68382-662-06	68382-662	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-662-06)
68382-662-10	68382-662	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-662-10)
68382-662-16	68382-662	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-662-16)
68382-662-30	68382-662	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	100 mg/1	10 BLISTER PACK in 1 CARTON (68382-662-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
51655-636-26	51655-636	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET	ORAL	20230120	N/A	ANDA	ANDA205936	Northwind Pharmaceuticals, LLC	SPIRONOLACTONE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-636-26)
51655-636-52	51655-636	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET	ORAL	20230614	N/A	ANDA	ANDA205936	Northwind Pharmaceuticals, LLC	SPIRONOLACTONE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-636-52)
60687-487-01	60687-487	HUMAN PRESCRIPTION DRUG	Spironolactone	Spironolactone	TABLET	ORAL	20190606	N/A	ANDA	ANDA205936	American Health Packaging	SPIRONOLACTONE	100 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-487-01) / 1 TABLET in 1 BLISTER PACK (60687-487-11)
70771-1027-0	70771-1027	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1027-0)
70771-1027-1	70771-1027	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1027-1)