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
47335-715-08	47335-715	HUMAN PRESCRIPTION DRUG	FINASTERIDE	FINASTERIDE	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA090507	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-715-08)
47335-715-13	47335-715	HUMAN PRESCRIPTION DRUG	FINASTERIDE	FINASTERIDE	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA090507	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (47335-715-13)
47335-715-18	47335-715	HUMAN PRESCRIPTION DRUG	FINASTERIDE	FINASTERIDE	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA090507	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-715-18)
47335-715-81	47335-715	HUMAN PRESCRIPTION DRUG	FINASTERIDE	FINASTERIDE	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA090507	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (47335-715-81)
47335-715-83	47335-715	HUMAN PRESCRIPTION DRUG	FINASTERIDE	FINASTERIDE	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA090507	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-715-83)
47335-715-88	47335-715	HUMAN PRESCRIPTION DRUG	FINASTERIDE	FINASTERIDE	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA090507	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-715-88)