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
72578-114-01	72578-114	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72578-114-01)
72578-114-05	72578-114	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72578-114-05)
72578-114-06	72578-114	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-114-06)
72578-115-06	72578-115	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-115-06)
72578-115-05	72578-115	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72578-115-05)
72578-115-01	72578-115	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72578-115-01)
72578-113-01	72578-113	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72578-113-01)
72578-113-05	72578-113	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72578-113-05)
72578-113-06	72578-113	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-113-06)
70771-1760-1	70771-1760	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1760-1)
70771-1760-3	70771-1760	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1760-3)
70771-1760-5	70771-1760	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	2.5 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1760-5)
70771-1761-1	70771-1761	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1761-1)
70771-1761-3	70771-1761	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1761-3)
70771-1761-5	70771-1761	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	5 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1761-5)
70771-1762-1	70771-1762	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1762-1)
70771-1762-3	70771-1762	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1762-3)
70771-1762-5	70771-1762	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate and Hydrochlorothiazide	bisoprolol fumarate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20230301	N/A	ANDA	ANDA215666	Zydus Lifesciences Limited	BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE	10 mg/1; 6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70771-1762-5)