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
31722-526-90	31722-526	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20130701	N/A	ANDA	ANDA090060	Camber Pharmaceuticals, Inc.	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-526-90)
31722-526-30	31722-526	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20130701	N/A	ANDA	ANDA090060	Camber Pharmaceuticals, Inc.	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-526-30)
31722-526-10	31722-526	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20130701	N/A	ANDA	ANDA090060	Camber Pharmaceuticals, Inc.	FINASTERIDE	1 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (31722-526-10)
76420-074-30	76420-074	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20200104	N/A	ANDA	ANDA090060	Asclemed USA, Inc.	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-074-30)
43598-390-30	43598-390	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20140610	N/A	ANDA	ANDA090060	Dr Reddys Laboratories Inc	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43598-390-30)
43598-390-90	43598-390	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20140610	N/A	ANDA	ANDA090060	Dr Reddys Laboratories Inc	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (43598-390-90)