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
72578-111-01	72578-111	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA215680	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72578-111-01)
72578-111-06	72578-111	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA215680	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-111-06)
72578-112-01	72578-112	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA215680	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72578-112-01)
72578-112-06	72578-112	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA215680	Viona Pharmaceuticals Inc	BISOPROLOL FUMARATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-112-06)
70771-1727-1	70771-1727	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA215680	Zydus Lifesciences Limited	BISOPROLOL FUMARATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1727-1)
70771-1727-3	70771-1727	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA215680	Zydus Lifesciences Limited	BISOPROLOL FUMARATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1727-3)
70771-1726-1	70771-1726	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA215680	Zydus Lifesciences Limited	BISOPROLOL FUMARATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70771-1726-1)
70771-1726-3	70771-1726	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20220915	N/A	ANDA	ANDA215680	Zydus Lifesciences Limited	BISOPROLOL FUMARATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70771-1726-3)