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
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)
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)
68788-8749-1	68788-8749	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20241011	N/A	ANDA	ANDA078341	Preferred Pharmaceuticals Inc.	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-8749-1)
68788-8749-3	68788-8749	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20241011	N/A	ANDA	ANDA078341	Preferred Pharmaceuticals Inc.	FINASTERIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8749-3)
68788-8749-6	68788-8749	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20241011	N/A	ANDA	ANDA078341	Preferred Pharmaceuticals Inc.	FINASTERIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8749-6)
68788-8749-9	68788-8749	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20241011	N/A	ANDA	ANDA078341	Preferred Pharmaceuticals Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8749-9)
68071-3234-9	68071-3234	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20180122	N/A	ANDA	ANDA078341	NuCare Pharmaceuticals,Inc.	FINASTERIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3234-9)
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)
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)
50090-6940-1	50090-6940	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 (50090-6940-1)
50090-6940-2	50090-6940	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20231215	N/A	ANDA	ANDA078341	A-S Medication Solutions	FINASTERIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (50090-6940-2)