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
70518-3616-3	70518-3616	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20230510	N/A	ANDA	ANDA078341	REMEDYREPACK INC.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3616-3)
70518-3616-4	70518-3616	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20240125	N/A	ANDA	ANDA078341	REMEDYREPACK INC.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-4)
70518-3616-5	70518-3616	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20240807	N/A	ANDA	ANDA078341	REMEDYREPACK INC.	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3616-5)
71335-1530-1	71335-1530	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20211228	N/A	ANDA	ANDA078341	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1530-1)
71335-1530-2	71335-1530	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20200306	N/A	ANDA	ANDA078341	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1530-2)
71335-1530-3	71335-1530	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20211228	N/A	ANDA	ANDA078341	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1530-3)
71335-1530-4	71335-1530	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20200320	N/A	ANDA	ANDA078341	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1530-4)
71335-1530-5	71335-1530	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20211228	N/A	ANDA	ANDA078341	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71335-1530-5)
71335-1530-6	71335-1530	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20211228	N/A	ANDA	ANDA078341	Bryant Ranch Prepack	FINASTERIDE	5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1530-6)
68071-3417-3	68071-3417	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20230526	N/A	ANDA	ANDA078341	NuCare Pharmaceuticals,Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3417-3)
68071-1648-9	68071-1648	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20170609	N/A	ANDA	ANDA078341	NuCare Pharmaceuticals, Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-1648-9)
76420-154-30	76420-154	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20210728	N/A	ANDA	ANDA078341	Asclemed USA, Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-154-30)
76420-154-90	76420-154	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20210728	N/A	ANDA	ANDA078341	Asclemed USA, Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-154-90)