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
76282-412-30	76282-412	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20150522	N/A	ANDA	ANDA090061	Exelan Pharmaceuticals Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76282-412-30)
76282-412-90	76282-412	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20150522	N/A	ANDA	ANDA090061	Exelan Pharmaceuticals Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76282-412-90)
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)
68788-8377-3	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)
68788-8377-6	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)
50268-314-15	50268-314	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090061	AvPAK	FINASTERIDE	5 mg/1	50 BLISTER PACK in 1 BOX (50268-314-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-314-11)
55154-8083-0	55154-8083	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20150613	N/A	ANDA	ANDA090061	Cardinal Health 107, LLC	FINASTERIDE	5 mg/1	10 BLISTER PACK in 1 BAG (55154-8083-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK