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
55111-171-05	55111-171	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20130102	N/A	ANDA	ANDA076436	Dr. Reddy's Laboratories Limited	FINASTERIDE	1 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (55111-171-05)
55111-171-18	55111-171	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20130102	N/A	ANDA	ANDA076436	Dr. Reddy's Laboratories Limited	FINASTERIDE	1 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (55111-171-18)
55111-171-30	55111-171	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20130102	N/A	ANDA	ANDA076436	Dr. Reddy's Laboratories Limited	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55111-171-30)
55111-171-90	55111-171	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20130102	N/A	ANDA	ANDA076436	Dr. Reddy's Laboratories Limited	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (55111-171-90)