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
71610-287-45	71610-287	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA203512	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	50 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71610-287-45)
71610-288-30	71610-288	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA203512	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71610-288-30)
71610-288-45	71610-288	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA203512	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	100 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71610-288-45)
71610-288-60	71610-288	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20190531	N/A	ANDA	ANDA203512	Aphena Pharma Solutions - Tennessee, LLC	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-288-60)
70518-1314-3	70518-1314	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20200225	N/A	ANDA	ANDA203512	REMEDYREPACK INC.	SPIRONOLACTONE	25 mg/1	100 POUCH in 1 BOX (70518-1314-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-1314-4)
70518-1334-1	70518-1334	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20191218	N/A	ANDA	ANDA203512	REMEDYREPACK INC.	SPIRONOLACTONE	100 mg/1	100 POUCH in 1 BOX (70518-1334-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1334-2)
71205-146-30	71205-146	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA203512	Proficient Rx LP	SPIRONOLACTONE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-146-30)
0615-8221-39	0615-8221	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180910	20241231	ANDA	ANDA203512	NCS HealthCare of KY, LLC dba Vangard Labs	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8221-39)
43063-974-90	43063-974	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20190426	N/A	ANDA	ANDA203512	PD-Rx Pharmaceuticals, Inc.	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-974-90)
16714-637-03	16714-637	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20221118	N/A	ANDA	ANDA203512	NorthStar RxLLC	SPIRONOLACTONE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16714-637-03)
16714-638-02	16714-638	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20221118	N/A	ANDA	ANDA203512	NorthStar RxLLC	SPIRONOLACTONE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16714-638-02)
16714-638-01	16714-638	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20221118	N/A	ANDA	ANDA203512	NorthStar RxLLC	SPIRONOLACTONE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-638-01)
16714-637-01	16714-637	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20221118	N/A	ANDA	ANDA203512	NorthStar RxLLC	SPIRONOLACTONE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-637-01)
16714-637-02	16714-637	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20221118	N/A	ANDA	ANDA203512	NorthStar RxLLC	SPIRONOLACTONE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16714-637-02)
16714-639-01	16714-639	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20221118	N/A	ANDA	ANDA203512	NorthStar RxLLC	SPIRONOLACTONE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16714-639-01)
16714-639-02	16714-639	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20221118	N/A	ANDA	ANDA203512	NorthStar RxLLC	SPIRONOLACTONE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16714-639-02)
70518-1742-2	70518-1742	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20220919	N/A	ANDA	ANDA203512	REMEDYREPACK INC.	SPIRONOLACTONE	50 mg/1	100 POUCH in 1 BOX (70518-1742-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-1742-3)
70518-1746-1	70518-1746	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20220216	N/A	ANDA	ANDA203512	REMEDYREPACK INC.	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1746-1)
70518-1746-2	70518-1746	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20230404	N/A	ANDA	ANDA203512	REMEDYREPACK INC.	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1746-2)
70518-1746-0	70518-1746	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20181220	N/A	ANDA	ANDA203512	REMEDYREPACK INC.	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1746-0)