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
71610-470-53	71610-470	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20210407	N/A	ANDA	ANDA075805	Aphena Pharma Solutions - Tennessee, LLC	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71610-470-53)
71610-470-60	71610-470	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20201009	N/A	ANDA	ANDA075805	Aphena Pharma Solutions - Tennessee, LLC	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71610-470-60)
71610-470-80	71610-470	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20201009	N/A	ANDA	ANDA075805	Aphena Pharma Solutions - Tennessee, LLC	FAMOTIDINE	20 mg/1	180 TABLET in 1 BOTTLE, PLASTIC (71610-470-80)
63629-2014-1	63629-2014	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20210216	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	1000 TABLET in 1 BOTTLE (63629-2014-1)
63629-2015-1	63629-2015	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20210216	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	100 TABLET in 1 BOTTLE (63629-2015-1)
72789-027-30	72789-027	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20191211	N/A	ANDA	ANDA075805	PD-Rx Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-027-30)
72789-027-60	72789-027	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20191211	N/A	ANDA	ANDA075805	PD-Rx Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (72789-027-60)
63629-2782-1	63629-2782	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20050314	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	30 TABLET in 1 BOTTLE (63629-2782-1)
63629-2782-2	63629-2782	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20070626	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	60 TABLET in 1 BOTTLE (63629-2782-2)
63629-2782-3	63629-2782	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20070716	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	100 TABLET in 1 BOTTLE (63629-2782-3)
63629-2782-4	63629-2782	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20101214	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	90 TABLET in 1 BOTTLE (63629-2782-4)
63629-2782-5	63629-2782	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20130204	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	15 TABLET in 1 BOTTLE (63629-2782-5)
63629-2782-6	63629-2782	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20150504	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	120 TABLET in 1 BOTTLE (63629-2782-6)
63629-2782-7	63629-2782	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20240905	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	20 TABLET in 1 BOTTLE (63629-2782-7)
72162-1737-0	72162-1737	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20240917	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	1000 TABLET in 1 BOTTLE (72162-1737-0)
72162-1737-1	72162-1737	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20240917	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	40 mg/1	100 TABLET in 1 BOTTLE (72162-1737-1)
63629-7013-1	63629-7013	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20050314	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	30 TABLET in 1 BOTTLE (63629-7013-1)
63629-7013-2	63629-7013	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20070626	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE (63629-7013-2)
63629-7013-3	63629-7013	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20070716	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE (63629-7013-3)
63629-7013-4	63629-7013	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20101214	N/A	ANDA	ANDA075805	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	10 TABLET in 1 BOTTLE (63629-7013-4)