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
64980-710-03	64980-710	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20250711	N/A	ANDA	ANDA219044	Rising Pharma Holdings, Inc.	BISOPROLOL FUMARATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (64980-710-03)
64980-710-01	64980-710	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20250711	N/A	ANDA	ANDA219044	Rising Pharma Holdings, Inc.	BISOPROLOL FUMARATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (64980-710-01)
64980-709-03	64980-709	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20250711	N/A	ANDA	ANDA219044	Rising Pharma Holdings, Inc.	BISOPROLOL FUMARATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (64980-709-03)
64980-709-01	64980-709	HUMAN PRESCRIPTION DRUG	Bisoprolol Fumarate	Bisoprolol Fumarate	TABLET, FILM COATED	ORAL	20250711	N/A	ANDA	ANDA219044	Rising Pharma Holdings, Inc.	BISOPROLOL FUMARATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (64980-709-01)