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
68071-2306-8	68071-2306	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20201130	N/A	ANDA	ANDA075805	NuCare Pharmaceuticals,Inc.	FAMOTIDINE	20 mg/1	180 TABLET in 1 BOTTLE (68071-2306-8)
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)
72189-207-30	72189-207	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET	ORAL	20210603	N/A	ANDA	ANDA075805	direct rx	FAMOTIDINE	40 mg/1	30 TABLET in 1 BOTTLE (72189-207-30)
72189-207-90	72189-207	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET	ORAL	20210603	N/A	ANDA	ANDA075805	direct rx	FAMOTIDINE	40 mg/1	90 TABLET in 1 BOTTLE (72189-207-90)
63739-645-10	63739-645	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20150129	20260331	ANDA	ANDA075805	Mckesson Corporation DBA SKY Packaginng	FAMOTIDINE	20 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-645-10) / 10 TABLET in 1 BLISTER PACK
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)