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
72865-215-30	72865-215	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	Famotidine	TABLET, FILM COATED	ORAL	20211015	N/A	ANDA	ANDA215689	XLCare Pharmaceuticals, Inc.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72865-215-30)
72865-214-01	72865-214	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	Famotidine	TABLET, FILM COATED	ORAL	20211015	N/A	ANDA	ANDA215689	XLCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72865-214-01)
72865-214-05	72865-214	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	Famotidine	TABLET, FILM COATED	ORAL	20211015	N/A	ANDA	ANDA215689	XLCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72865-214-05)
72865-214-18	72865-214	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	Famotidine	TABLET, FILM COATED	ORAL	20211015	N/A	ANDA	ANDA215689	XLCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (72865-214-18)
72865-214-30	72865-214	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	Famotidine	TABLET, FILM COATED	ORAL	20211015	N/A	ANDA	ANDA215689	XLCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72865-214-30)
72865-215-18	72865-215	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	Famotidine	TABLET, FILM COATED	ORAL	20211015	N/A	ANDA	ANDA215689	XLCare Pharmaceuticals, Inc.	FAMOTIDINE	40 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (72865-215-18)
72865-215-05	72865-215	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	Famotidine	TABLET, FILM COATED	ORAL	20211015	N/A	ANDA	ANDA215689	XLCare Pharmaceuticals, Inc.	FAMOTIDINE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72865-215-05)
72865-215-01	72865-215	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	Famotidine	TABLET, FILM COATED	ORAL	20211015	N/A	ANDA	ANDA215689	XLCare Pharmaceuticals, Inc.	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72865-215-01)