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
71335-2805-4	71335-2805	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20251014	N/A	ANDA	ANDA217400	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2805-4)
71335-2805-8	71335-2805	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20251014	N/A	ANDA	ANDA217400	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-2805-8)
71335-2805-9	71335-2805	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20251014	N/A	ANDA	ANDA217400	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-2805-9)
71335-2805-5	71335-2805	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20251014	N/A	ANDA	ANDA217400	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2805-5)
71335-2805-6	71335-2805	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20251014	N/A	ANDA	ANDA217400	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-2805-6)
71335-2805-7	71335-2805	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20251014	N/A	ANDA	ANDA217400	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2805-7)
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)