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
47335-714-83	47335-714	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20221123	N/A	ANDA	ANDA090508	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-714-83)
47335-714-88	47335-714	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20221123	N/A	ANDA	ANDA090508	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-714-88)
47335-714-81	47335-714	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20221123	N/A	ANDA	ANDA090508	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (47335-714-81)
47335-714-18	47335-714	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20221123	N/A	ANDA	ANDA090508	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	1 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-714-18)
47335-714-08	47335-714	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20221123	N/A	ANDA	ANDA090508	Sun Pharmaceutical Industries, Inc.	FINASTERIDE	1 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-714-08)