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
42806-039-01	42806-039	HUMAN PRESCRIPTION DRUG	Betaxolol	Betaxolol	TABLET, FILM COATED	ORAL	20100720	N/A	ANDA	ANDA075541	Epic Pharma LLC	BETAXOLOL HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42806-039-01)
42806-039-10	42806-039	HUMAN PRESCRIPTION DRUG	Betaxolol	Betaxolol	TABLET, FILM COATED	ORAL	20100720	N/A	ANDA	ANDA075541	Epic Pharma LLC	BETAXOLOL HYDROCHLORIDE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42806-039-10)
24658-700-01	24658-700	HUMAN PRESCRIPTION DRUG	Betaxolol	Betaxolol	TABLET, FILM COATED	ORAL	20161215	N/A	ANDA	ANDA075541	PuraCap Laboratories LLC	BETAXOLOL HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (24658-700-01)
42806-038-01	42806-038	HUMAN PRESCRIPTION DRUG	Betaxolol	Betaxolol	TABLET, FILM COATED	ORAL	20100720	N/A	ANDA	ANDA075541	Epic Pharma LLC	BETAXOLOL HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42806-038-01)
42806-038-10	42806-038	HUMAN PRESCRIPTION DRUG	Betaxolol	Betaxolol	TABLET, FILM COATED	ORAL	20100720	N/A	ANDA	ANDA075541	Epic Pharma LLC	BETAXOLOL HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42806-038-10)
24658-701-01	24658-701	HUMAN PRESCRIPTION DRUG	Betaxolol	Betaxolol	TABLET, FILM COATED	ORAL	20161215	N/A	ANDA	ANDA075541	PuraCap Laboratories LLC	BETAXOLOL HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (24658-701-01)