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
68788-8377-9	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)
76282-412-05	76282-412	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20150522	N/A	ANDA	ANDA090061	Exelan Pharmaceuticals Inc.	FINASTERIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76282-412-05)
76282-412-10	76282-412	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20150522	N/A	ANDA	ANDA090061	Exelan Pharmaceuticals Inc.	FINASTERIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (76282-412-10)
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)
0904-6830-06	0904-6830	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20150613	N/A	ANDA	ANDA090061	Major Pharmaceuticals	FINASTERIDE	5 mg/1	50 BLISTER PACK in 1 CARTON (0904-6830-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-6830-61	0904-6830	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20150613	N/A	ANDA	ANDA090061	Major Pharmaceuticals	FINASTERIDE	5 mg/1	100 BLISTER PACK in 1 CARTON (0904-6830-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK