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
72789-392-82	72789-392	HUMAN PRESCRIPTION DRUG	BISOPROLOL FUMARATE	BISOPROLOL FUMARATE	TABLET, FILM COATED	ORAL	20240417	N/A	ANDA	ANDA217617	PD-Rx Pharmaceuticals, Inc.	BISOPROLOL FUMARATE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-392-82)
72789-395-82	72789-395	HUMAN PRESCRIPTION DRUG	BISOPROLOL FUMARATE	BISOPROLOL FUMARATE	TABLET, FILM COATED	ORAL	20240417	N/A	ANDA	ANDA217617	PD-Rx Pharmaceuticals, Inc.	BISOPROLOL FUMARATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-395-82)
70095-019-01	70095-019	HUMAN PRESCRIPTION DRUG	BISOPROLOL FUMARATE	BISOPROLOL FUMARATE	TABLET, FILM COATED	ORAL	20240310	N/A	ANDA	ANDA217617	Sun Pharmaceutical Industries Limited	BISOPROLOL FUMARATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-019-01)
70095-019-02	70095-019	HUMAN PRESCRIPTION DRUG	BISOPROLOL FUMARATE	BISOPROLOL FUMARATE	TABLET, FILM COATED	ORAL	20240310	N/A	ANDA	ANDA217617	Sun Pharmaceutical Industries Limited	BISOPROLOL FUMARATE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70095-019-02)
70095-020-01	70095-020	HUMAN PRESCRIPTION DRUG	BISOPROLOL FUMARATE	BISOPROLOL FUMARATE	TABLET, FILM COATED	ORAL	20240310	N/A	ANDA	ANDA217617	Sun Pharmaceutical Industries Limited	BISOPROLOL FUMARATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-020-01)
70095-020-02	70095-020	HUMAN PRESCRIPTION DRUG	BISOPROLOL FUMARATE	BISOPROLOL FUMARATE	TABLET, FILM COATED	ORAL	20240310	N/A	ANDA	ANDA217617	Sun Pharmaceutical Industries Limited	BISOPROLOL FUMARATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70095-020-02)