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
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)
68788-8889-3	68788-8889	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250923	N/A	ANDA	ANDA075718	Preferred Pharmaceuticals Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8889-3)
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)
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)
71335-1950-8	71335-1950	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20260331	N/A	ANDA	ANDA075718	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-1950-8)
71335-1950-9	71335-1950	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20260331	N/A	ANDA	ANDA075718	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-1950-9)
82804-194-10	82804-194	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250528	N/A	ANDA	ANDA075718	Proficient Rx LP	FAMOTIDINE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (82804-194-10)
82804-194-30	82804-194	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250425	N/A	ANDA	ANDA075718	Proficient Rx LP	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82804-194-30)
82804-194-60	82804-194	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20260423	N/A	ANDA	ANDA075718	Proficient Rx LP	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (82804-194-60)
82804-194-78	82804-194	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250605	N/A	ANDA	ANDA075718	Proficient Rx LP	FAMOTIDINE	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (82804-194-78)
82804-194-90	82804-194	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250204	N/A	ANDA	ANDA075718	Proficient Rx LP	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-194-90)
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