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
64980-624-01	64980-624	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA218181	Rising Pharma Holdings, Inc.	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (64980-624-01)
64980-624-10	64980-624	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA218181	Rising Pharma Holdings, Inc.	FAMOTIDINE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (64980-624-10)
64980-624-50	64980-624	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA218181	Rising Pharma Holdings, Inc.	FAMOTIDINE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (64980-624-50)
64980-623-01	64980-623	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA218181	Rising Pharma Holdings, Inc.	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (64980-623-01)
64980-623-10	64980-623	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA218181	Rising Pharma Holdings, Inc.	FAMOTIDINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (64980-623-10)
64980-623-50	64980-623	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA218181	Rising Pharma Holdings, Inc.	FAMOTIDINE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (64980-623-50)