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
50090-6932-0	50090-6932	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20231214	N/A	ANDA	ANDA075511	A-S Medication Solutions	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6932-0)
71205-276-30	71205-276	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-276-30)
71205-276-67	71205-276	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20240923	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	20 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (71205-276-67)
71205-276-78	71205-276	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20250710	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	20 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71205-276-78)
71205-276-10	71205-276	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-276-10)
71205-276-06	71205-276	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20210708	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	20 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71205-276-06)
71205-276-60	71205-276	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-276-60)
67296-1121-3	67296-1121	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA075511	RedPharm Drug, Inc.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1121-3)
71205-781-30	71205-781	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20230327	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-781-30)
71205-781-60	71205-781	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20230327	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-781-60)
71205-781-90	71205-781	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20230327	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)
50090-1044-0	50090-1044	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA075511	A-S Medication Solutions	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-1044-0)
50090-1044-1	50090-1044	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA075511	A-S Medication Solutions	FAMOTIDINE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-1044-1)
45865-881-51	45865-881	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA075511	Medsource Pharmaceuticals	FAMOTIDINE	20 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (45865-881-51)
45865-881-60	45865-881	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA075511	Medsource Pharmaceuticals	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (45865-881-60)
50090-1044-2	50090-1044	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA075511	A-S Medication Solutions	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-1044-2)
50090-1044-3	50090-1044	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20181005	N/A	ANDA	ANDA075511	A-S Medication Solutions	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-1044-3)
51655-233-25	51655-233	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221206	N/A	ANDA	ANDA075511	Northwind Pharmaceuticals, LLC	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-25)
51655-233-26	51655-233	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220817	N/A	ANDA	ANDA075511	Northwind Pharmaceuticals, LLC	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-26)
51655-233-52	51655-233	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20221005	N/A	ANDA	ANDA075511	Northwind Pharmaceuticals, LLC	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-52)