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
71335-1634-4	71335-1634	HUMAN PRESCRIPTION DRUG	Finasteride	finasteride	TABLET, FILM COATED	ORAL	20200610	N/A	ANDA	ANDA090121	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1634-4)
71335-1634-5	71335-1634	HUMAN PRESCRIPTION DRUG	Finasteride	finasteride	TABLET, FILM COATED	ORAL	20200610	N/A	ANDA	ANDA090121	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71335-1634-5)
71335-1634-6	71335-1634	HUMAN PRESCRIPTION DRUG	Finasteride	finasteride	TABLET, FILM COATED	ORAL	20200610	N/A	ANDA	ANDA090121	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1634-6)
68071-3354-9	68071-3354	HUMAN PRESCRIPTION DRUG	Finasteride	finasteride	TABLET, FILM COATED	ORAL	20170720	N/A	ANDA	ANDA090121	NuCare Pharmaceuticals,Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3354-9)