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
72205-146-99	72205-146	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240918	N/A	ANDA	ANDA217400	Novadoz Pharmaceuticals LLC	FAMOTIDINE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72205-146-99)
70518-4395-0	70518-4395	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA217400	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4395-0)
70518-4395-1	70518-4395	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20260423	N/A	ANDA	ANDA217400	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	50 POUCH in 1 BOX (70518-4395-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-4395-2)
68788-4021-3	68788-4021	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250905	N/A	ANDA	ANDA217400	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-4021-3)
68788-4021-4	68788-4021	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250905	N/A	ANDA	ANDA217400	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (68788-4021-4)
68788-4021-6	68788-4021	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250905	N/A	ANDA	ANDA217400	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-4021-6)
68788-4021-9	68788-4021	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250905	N/A	ANDA	ANDA217400	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-4021-9)
67296-2186-3	67296-2186	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240918	N/A	ANDA	ANDA217400	Redpharm Drug	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-2186-3)