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
68788-7019-3	68788-7019	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20171011	N/A	ANDA	ANDA203512	Preferred Pharmaceuticals Inc.	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7019-3)
68788-7019-6	68788-7019	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20171011	N/A	ANDA	ANDA203512	Preferred Pharmaceuticals Inc.	SPIRONOLACTONE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7019-6)
68788-7019-9	68788-7019	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20171011	N/A	ANDA	ANDA203512	Preferred Pharmaceuticals Inc.	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7019-9)
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)
71205-147-30	71205-147	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA203512	Proficient Rx LP	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-147-30)
71205-147-60	71205-147	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA203512	Proficient Rx LP	SPIRONOLACTONE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-147-60)
71205-147-90	71205-147	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20181101	N/A	ANDA	ANDA203512	Proficient Rx LP	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-147-90)
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)
43063-832-01	43063-832	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180131	N/A	ANDA	ANDA203512	PD-Rx Pharmaceuticals, Inc.	SPIRONOLACTONE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-01)
43063-832-30	43063-832	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20180131	N/A	ANDA	ANDA203512	PD-Rx Pharmaceuticals, Inc.	SPIRONOLACTONE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-832-30)
53002-2707-3	53002-2707	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20221101	N/A	ANDA	ANDA203512	RPK Pharmaceuticals, Inc.	SPIRONOLACTONE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-2707-3)
71335-0304-1	71335-0304	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA203512	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0304-1)
16729-225-01	16729-225	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170602	N/A	ANDA	ANDA203512	Accord Healthcare, Inc.	SPIRONOLACTONE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16729-225-01)
16729-225-16	16729-225	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170602	N/A	ANDA	ANDA203512	Accord Healthcare, Inc.	SPIRONOLACTONE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16729-225-16)
16729-225-17	16729-225	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170615	N/A	ANDA	ANDA203512	Accord Healthcare, Inc.	SPIRONOLACTONE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16729-225-17)
71335-0304-2	71335-0304	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA203512	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (71335-0304-2)
71335-0304-3	71335-0304	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA203512	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0304-3)
71335-0304-4	71335-0304	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA203512	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0304-4)
71335-0304-5	71335-0304	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA203512	Bryant Ranch Prepack	SPIRONOLACTONE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0304-5)
68071-3375-1	68071-3375	HUMAN PRESCRIPTION DRUG	Spironolactone	spironolactone	TABLET, FILM COATED	ORAL	20170711	N/A	ANDA	ANDA203512	NuCare Pharmaceuticals, Inc.	SPIRONOLACTONE	25 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68071-3375-1)