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
55111-119-30	55111-119	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075718	Dr.Reddy's Laboratories Limited	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55111-119-30)
68788-8889-6	68788-8889	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA075718	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8889-6)
68788-8889-9	68788-8889	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA075718	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8889-9)
68788-8889-1	68788-8889	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA075718	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-8889-1)
67296-1859-5	67296-1859	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075718	Redpharm Drug, Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1859-5)
67296-1859-8	67296-1859	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075718	Redpharm Drug, Inc.	FAMOTIDINE	20 mg/1	25 TABLET, FILM COATED in 1 BOTTLE (67296-1859-8)
55154-4313-0	55154-4313	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20230315	N/A	ANDA	ANDA075718	Cardinal Health 107, LLC	FAMOTIDINE	20 mg/1	10 BLISTER PACK in 1 BAG (55154-4313-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
50268-299-15	50268-299	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220525	N/A	ANDA	ANDA075718	AvPAK	FAMOTIDINE	20 mg/1	50 BLISTER PACK in 1 BOX (50268-299-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-299-11)
83008-091-30	83008-091	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240918	20261231	ANDA	ANDA075718	Quality Care Products, LLC	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (83008-091-30)
55154-2628-0	55154-2628	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20230809	N/A	ANDA	ANDA075718	Cardinal Health 107, LLC	FAMOTIDINE	20 mg/1	10 BLISTER PACK in 1 BAG (55154-2628-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7193-06	0904-7193	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220810	N/A	ANDA	ANDA075718	Major Pharmaceuticals	FAMOTIDINE	20 mg/1	50 BLISTER PACK in 1 CARTON (0904-7193-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7193-61	0904-7193	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075718	Major Pharmaceuticals	FAMOTIDINE	20 mg/1	100 BLISTER PACK in 1 CARTON (0904-7193-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
68645-594-59	68645-594	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210922	N/A	ANDA	ANDA075718	Legacy Pharmaceutical Packaging, LLC	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68645-594-59)