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
16729-089-10	16729-089	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20131108	N/A	ANDA	ANDA091643	Accord Healthcare, Inc.	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (16729-089-10)
16729-089-15	16729-089	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20140117	N/A	ANDA	ANDA091643	Accord Healthcare, Inc.	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (16729-089-15)
63187-863-20	63187-863	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20220211	N/A	ANDA	ANDA091643	Proficient Rx LP	FINASTERIDE	1 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63187-863-20)
63187-863-30	63187-863	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20170601	N/A	ANDA	ANDA091643	Proficient Rx LP	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-863-30)
63187-863-60	63187-863	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20170601	N/A	ANDA	ANDA091643	Proficient Rx LP	FINASTERIDE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-863-60)
63187-863-90	63187-863	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20170601	N/A	ANDA	ANDA091643	Proficient Rx LP	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-863-90)
71713-096-90	71713-096	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20190612	N/A	ANDA	ANDA091643	Thirty Madison Inc	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71713-096-90)