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
65862-149-01	65862-149	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20071030	N/A	ANDA	ANDA078341	Aurobindo Pharma Limited	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-149-01)
65862-149-05	65862-149	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20071030	N/A	ANDA	ANDA078341	Aurobindo Pharma Limited	FINASTERIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-149-05)
65862-149-30	65862-149	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20071030	N/A	ANDA	ANDA078341	Aurobindo Pharma Limited	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-149-30)
65862-149-90	65862-149	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20071030	N/A	ANDA	ANDA078341	Aurobindo Pharma Limited	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-149-90)
50090-6941-0	50090-6941	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20231215	N/A	ANDA	ANDA078341	A-S Medication Solutions	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6941-0)
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)
82009-061-05	82009-061	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20221121	N/A	ANDA	ANDA078341	QUALLENT PHARMACEUTICALS HEALTH LLC	FINASTERIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05)
60687-428-01	60687-428	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20190909	N/A	ANDA	ANDA078341	American Health Packaging	FINASTERIDE	5 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-428-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-428-11)
60687-428-65	60687-428	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20200120	N/A	ANDA	ANDA078341	American Health Packaging	FINASTERIDE	5 mg/1	50 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-428-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-428-11)
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)
70518-1704-1	70518-1704	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20240219	N/A	ANDA	ANDA078341	REMEDYREPACK INC.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1704-1)
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)
57237-062-05	57237-062	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20071030	N/A	ANDA	ANDA078341	Rising Pharma Holdings, Inc.	FINASTERIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (57237-062-05)
57237-062-30	57237-062	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20071030	N/A	ANDA	ANDA078341	Rising Pharma Holdings, Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (57237-062-30)
57237-062-90	57237-062	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20071030	N/A	ANDA	ANDA078341	Rising Pharma Holdings, Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (57237-062-90)
50090-6940-0	50090-6940	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20231215	N/A	ANDA	ANDA078341	A-S Medication Solutions	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6940-0)