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
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)
68071-3201-2	68071-3201	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20170324	N/A	ANDA	ANDA078916	NuCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	20 TABLET in 1 BOTTLE (68071-3201-2)
68071-3201-3	68071-3201	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20170324	N/A	ANDA	ANDA078916	NuCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	30 TABLET in 1 BOTTLE (68071-3201-3)
68071-3201-6	68071-3201	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20170324	N/A	ANDA	ANDA078916	NuCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE (68071-3201-6)
68071-3201-8	68071-3201	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20170324	N/A	ANDA	ANDA078916	NuCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	180 TABLET in 1 BOTTLE (68071-3201-8)
68071-3201-9	68071-3201	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20170324	N/A	ANDA	ANDA078916	NuCare Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE (68071-3201-9)
46708-293-30	46708-293	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160129	N/A	ANDA	ANDA078916	Alembic Pharmaceuticals Limited	FAMOTIDINE	20 mg/1	30 TABLET in 1 BOTTLE (46708-293-30)
71335-0231-2	71335-0231	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20180306	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	60 TABLET in 1 BOTTLE (71335-0231-2)
71335-0231-3	71335-0231	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20191111	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	100 TABLET in 1 BOTTLE (71335-0231-3)
71335-0231-4	71335-0231	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20180716	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	90 TABLET in 1 BOTTLE (71335-0231-4)
71335-0231-5	71335-0231	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20190131	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	15 TABLET in 1 BOTTLE (71335-0231-5)
71335-0231-6	71335-0231	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20211227	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	120 TABLET in 1 BOTTLE (71335-0231-6)
71335-0231-7	71335-0231	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20211227	N/A	ANDA	ANDA078916	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	20 TABLET in 1 BOTTLE (71335-0231-7)
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)