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
68382-660-05	68382-660	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-660-05)
68382-660-06	68382-660	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-660-06)
68382-660-10	68382-660	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-660-10)
68382-660-16	68382-660	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-660-16)
68382-660-30	68382-660	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Pharmaceuticals (USA) Inc.	SPIRONOLACTONE	25 mg/1	10 BLISTER PACK in 1 CARTON (68382-660-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70518-4512-0	70518-4512	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20251028	N/A	ANDA	ANDA205936	REMEDYREPACK INC.	SPIRONOLACTONE	100 mg/1	100 POUCH in 1 BOX (70518-4512-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4512-1)