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
0093-7355-56	0093-7355	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20061215	N/A	ANDA	ANDA076511	Teva Pharmaceuticals USA, Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-7355-56)
0093-7355-98	0093-7355	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20070222	N/A	ANDA	ANDA076511	Teva Pharmaceuticals USA, Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0093-7355-98)
70518-3612-0	70518-3612	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20230108	N/A	ANDA	ANDA076511	REMEDYREPACK INC.	FINASTERIDE	5 mg/1	30 POUCH in 1 BOX (70518-3612-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3612-1)
0093-7355-05	0093-7355	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20080314	N/A	ANDA	ANDA076511	Teva Pharmaceuticals USA, Inc.	FINASTERIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-7355-05)