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
35573-400-99	35573-400	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20180713	N/A	ANDA	ANDA203687	Burel Pharmaceuticals, LLC	FINASTERIDE	1 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (35573-400-99)
65862-927-30	65862-927	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20140920	N/A	ANDA	ANDA203687	Aurobindo Pharma Limited	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-927-30)
65862-927-90	65862-927	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20140920	N/A	ANDA	ANDA203687	Aurobindo Pharma Limited	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-927-90)
65862-927-99	65862-927	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20140920	N/A	ANDA	ANDA203687	Aurobindo Pharma Limited	FINASTERIDE	1 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-927-99)
68788-6875-3	68788-6875	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20170123	N/A	ANDA	ANDA203687	Preferred Pharmaceuticals Inc.	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-6875-3)
68788-6875-6	68788-6875	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20170123	N/A	ANDA	ANDA203687	Preferred Pharmaceuticals Inc.	FINASTERIDE	1 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-6875-6)
68788-6875-9	68788-6875	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20170123	N/A	ANDA	ANDA203687	Preferred Pharmaceuticals Inc.	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-6875-9)
57237-061-30	57237-061	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20131105	N/A	ANDA	ANDA203687	Rising Health, LLC	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (57237-061-30)
57237-061-90	57237-061	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20131105	N/A	ANDA	ANDA203687	Rising Health, LLC	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (57237-061-90)
76420-151-30	76420-151	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20220118	N/A	ANDA	ANDA203687	Asclemed USA, Inc.	FINASTERIDE	1 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-151-30)
76420-151-90	76420-151	HUMAN PRESCRIPTION DRUG	Finasteride	Finasteride	TABLET, FILM COATED	ORAL	20220118	N/A	ANDA	ANDA203687	Asclemed USA, Inc.	FINASTERIDE	1 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-151-90)