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
50090-6030-0	50090-6030	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220706	N/A	ANDA	ANDA215995	A-S Medication Solutions	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6030-0)
68462-878-01	68462-878	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-878-01)
68462-878-05	68462-878	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-878-05)
68462-878-30	68462-878	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-878-30)
68462-879-01	68462-879	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-879-01)
68462-879-05	68462-879	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-879-05)
68462-879-30	68462-879	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-879-30)
68462-880-01	68462-880	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68462-880-01)
68462-880-05	68462-880	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-880-05)
68462-880-30	68462-880	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	Bisoprolol Fumarate and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220126	N/A	ANDA	ANDA215995	GLENMARK PHARMACEUTICALS INC., USA	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-880-30)