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
0615-8562-05	0615-8562	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET	ORAL	20250211	N/A	ANDA	ANDA076437	NCS HealthCare of KY, LLC dba Vangard Labs	FINASTERIDE	5 mg/1	15 TABLET in 1 BLISTER PACK (0615-8562-05)
0615-8562-39	0615-8562	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET	ORAL	20250211	N/A	ANDA	ANDA076437	NCS HealthCare of KY, LLC dba Vangard Labs	FINASTERIDE	5 mg/1	30 TABLET in 1 BLISTER PACK (0615-8562-39)
55111-172-01	55111-172	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET	ORAL	20070228	N/A	ANDA	ANDA076437	Dr. Reddy's Laboratories Limited	FINASTERIDE	5 mg/1	100 TABLET in 1 BOTTLE (55111-172-01)
55111-172-05	55111-172	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET	ORAL	20070228	N/A	ANDA	ANDA076437	Dr. Reddy's Laboratories Limited	FINASTERIDE	5 mg/1	500 TABLET in 1 BOTTLE (55111-172-05)
55111-172-30	55111-172	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET	ORAL	20070228	N/A	ANDA	ANDA076437	Dr. Reddy's Laboratories Limited	FINASTERIDE	5 mg/1	30 TABLET in 1 BOTTLE (55111-172-30)
55111-172-78	55111-172	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET	ORAL	20070228	N/A	ANDA	ANDA076437	Dr. Reddy's Laboratories Limited	FINASTERIDE	5 mg/1	10 BLISTER PACK in 1 CARTON (55111-172-78) / 10 TABLET in 1 BLISTER PACK (55111-172-79)
55111-172-90	55111-172	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET	ORAL	20070228	N/A	ANDA	ANDA076437	Dr. Reddy's Laboratories Limited	FINASTERIDE	5 mg/1	90 TABLET in 1 BOTTLE (55111-172-90)