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
50090-6478-0	50090-6478	HUMAN PRESCRIPTION DRUG	bisoprolol fumarate and hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230516	N/A	NDA AUTHORIZED GENERIC	NDA020186	A-S Medication Solutions	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6478-0)
0093-3241-01	0093-3241	HUMAN PRESCRIPTION DRUG	bisoprolol fumarate and hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190807	N/A	NDA AUTHORIZED GENERIC	NDA020186	Teva Pharmaceuticals USA, Inc.	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-3241-01)
0093-3242-01	0093-3242	HUMAN PRESCRIPTION DRUG	bisoprolol fumarate and hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190807	N/A	NDA AUTHORIZED GENERIC	NDA020186	Teva Pharmaceuticals USA, Inc.	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-3242-01)
0093-3243-56	0093-3243	HUMAN PRESCRIPTION DRUG	bisoprolol fumarate and hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20190807	N/A	NDA AUTHORIZED GENERIC	NDA020186	Teva Pharmaceuticals USA, Inc.	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-3243-56)