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
51655-233-26	51655-233	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20220817	N/A	ANDA	ANDA075511	Northwind Health Company, 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 Health Company, LLC	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-52)
43063-533-30	43063-533	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20140414	N/A	ANDA	ANDA075511	PD-Rx Pharmaceuticals, Inc.	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-533-30)
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)
71205-276-10	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)