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
71610-515-53	71610-515	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090061	Aphena Pharma Solutions - Tennessee, LLC	FINASTERIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-515-53)
68788-8377-3	68788-8377	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20230228	N/A	ANDA	ANDA090061	Preferred Pharmaceuticals, Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8377-3)
68788-8377-1	68788-8377	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20230228	N/A	ANDA	ANDA090061	Preferred Pharmaceuticals, Inc.	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-8377-1)
68788-8377-6	68788-8377	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20230228	N/A	ANDA	ANDA090061	Preferred Pharmaceuticals, Inc.	FINASTERIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8377-6)
68788-8377-9	68788-8377	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20230228	N/A	ANDA	ANDA090061	Preferred Pharmaceuticals, Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8377-9)
50090-7228-0	50090-7228	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20240822	N/A	ANDA	ANDA090061	A-S Medication Solutions	FINASTERIDE	5 mg/1	12 BOTTLE in 1 CASE (50090-7228-0) / 30 TABLET, FILM COATED in 1 BOTTLE
43598-303-30	43598-303	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20121025	N/A	ANDA	ANDA090061	Dr Reddys Laboratories Inc	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43598-303-30)
43598-303-90	43598-303	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20121025	N/A	ANDA	ANDA090061	Dr Reddys Laboratories Inc	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (43598-303-90)