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
71335-9748-8	71335-9748	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240405	N/A	ANDA	ANDA215630	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-9748-8)
71335-9748-9	71335-9748	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20240405	N/A	ANDA	ANDA215630	Bryant Ranch Prepack	FAMOTIDINE	20 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-9748-9)
50090-6582-0	50090-6582	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230809	N/A	ANDA	ANDA215630	A-S Medication Solutions	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6582-0)
50090-6582-1	50090-6582	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230809	N/A	ANDA	ANDA215630	A-S Medication Solutions	FAMOTIDINE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-6582-1)
50090-6582-2	50090-6582	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230809	N/A	ANDA	ANDA215630	A-S Medication Solutions	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-6582-2)
50090-6582-3	50090-6582	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230809	N/A	ANDA	ANDA215630	A-S Medication Solutions	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6582-3)
67877-889-01	67877-889	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230823	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-889-01)
67877-889-05	67877-889	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20230823	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-889-05)
67877-842-05	67877-842	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20250203	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-842-05)
67877-842-10	67877-842	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20220708	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (67877-842-10)
67877-842-01	67877-842	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20220708	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-842-01)
67877-843-05	67877-843	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20220708	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-843-05)
67877-843-01	67877-843	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET, FILM COATED	ORAL	20220708	N/A	ANDA	ANDA215630	Ascend Laboratories, LLC	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-843-01)