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
70771-1028-0	70771-1028	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (70771-1028-0)
70771-1028-1	70771-1028	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1028-1)
70771-1028-3	70771-1028	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1028-3)
70771-1028-4	70771-1028	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	50 mg/1	10 BLISTER PACK in 1 CARTON (70771-1028-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1028-5	70771-1028	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1028-5)
70771-1028-9	70771-1028	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1028-9)
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
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)
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)
70771-1027-3	70771-1027	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1027-3)
70771-1027-4	70771-1027	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	25 mg/1	10 BLISTER PACK in 1 CARTON (70771-1027-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1027-5	70771-1027	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1027-5)
70771-1027-9	70771-1027	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA205936	Zydus Lifesciences Limited	SPIRONOLACTONE	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70771-1027-9)
70518-4470-0	70518-4470	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20250908	N/A	ANDA	ANDA205936	REMEDYREPACK INC.	SPIRONOLACTONE	25 mg/1	100 POUCH in 1 BOX (70518-4470-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4470-1)
51655-861-26	51655-861	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET	ORAL	20230215	N/A	ANDA	ANDA205936	Northwind Pharmaceuticals, LLC	SPIRONOLACTONE	50 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-861-26)
51655-861-52	51655-861	HUMAN PRESCRIPTION DRUG	spironolactone	spironolactone	TABLET	ORAL	20230630	N/A	ANDA	ANDA205936	Northwind Pharmaceuticals, LLC	SPIRONOLACTONE	50 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-861-52)
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)