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
71335-0409-1	71335-0409	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20220209	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	30 TABLET in 1 BOTTLE (71335-0409-1)
71335-0409-2	71335-0409	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20220209	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE (71335-0409-2)
71335-0409-3	71335-0409	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20220209	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	20 TABLET in 1 BOTTLE (71335-0409-3)
71335-0409-4	71335-0409	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20220209	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE (71335-0409-4)
71335-0409-5	71335-0409	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20220209	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	100 TABLET in 1 BOTTLE (71335-0409-5)
71335-0409-6	71335-0409	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20220209	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	10 TABLET in 1 BOTTLE (71335-0409-6)
71335-0409-7	71335-0409	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20220209	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	120 TABLET in 1 BOTTLE (71335-0409-7)
71335-0409-8	71335-0409	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20220209	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	50 TABLET in 1 BOTTLE (71335-0409-8)
82868-077-30	82868-077	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20251126	N/A	ANDA	ANDA078916	Northwind Health Company, LLC	FAMOTIDINE	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (82868-077-30)
82868-077-60	82868-077	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20250723	N/A	ANDA	ANDA078916	Northwind Health Company, LLC	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (82868-077-60)
82868-077-90	82868-077	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20250422	N/A	ANDA	ANDA078916	Northwind Health Company, LLC	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (82868-077-90)
63187-723-00	63187-723	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160601	N/A	ANDA	ANDA078916	Proficient Rx LP	FAMOTIDINE	20 mg/1	100 TABLET in 1 BOTTLE (63187-723-00)
63187-723-06	63187-723	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20190901	N/A	ANDA	ANDA078916	Proficient Rx LP	FAMOTIDINE	20 mg/1	6 TABLET in 1 BOTTLE (63187-723-06)
63187-723-10	63187-723	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20161101	N/A	ANDA	ANDA078916	Proficient Rx LP	FAMOTIDINE	20 mg/1	10 TABLET in 1 BOTTLE (63187-723-10)
63187-723-30	63187-723	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160601	N/A	ANDA	ANDA078916	Proficient Rx LP	FAMOTIDINE	20 mg/1	30 TABLET in 1 BOTTLE (63187-723-30)
63187-723-60	63187-723	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160601	N/A	ANDA	ANDA078916	Proficient Rx LP	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE (63187-723-60)
63187-723-90	63187-723	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160601	N/A	ANDA	ANDA078916	Proficient Rx LP	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE (63187-723-90)
72189-141-60	72189-141	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET	ORAL	20201015	N/A	ANDA	ANDA078916	direct rx	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE (72189-141-60)
72189-141-90	72189-141	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET	ORAL	20201015	N/A	ANDA	ANDA078916	direct rx	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE (72189-141-90)
63187-908-30	63187-908	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20170901	N/A	ANDA	ANDA078916	Proficient Rx LP	FAMOTIDINE	40 mg/1	30 TABLET in 1 BOTTLE (63187-908-30)