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
0378-0501-01	0378-0501	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210222	N/A	ANDA	ANDA075768	Mylan Pharmaceuticals Inc.	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0501-01)
70518-3207-0	70518-3207	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210830	N/A	ANDA	ANDA075768	REMEDYREPACK INC.	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3207-0)
0378-0505-01	0378-0505	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210222	N/A	ANDA	ANDA075768	Mylan Pharmaceuticals Inc.	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0505-01)
70518-3333-0	70518-3333	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20220113	N/A	ANDA	ANDA075768	REMEDYREPACK INC.	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3333-0)
0378-0503-01	0378-0503	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20210222	N/A	ANDA	ANDA075768	Mylan Pharmaceuticals Inc.	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0503-01)