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
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)
51655-102-26	51655-102	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20230125	N/A	ANDA	ANDA075511	Northwind Pharmaceuticals	FAMOTIDINE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-102-26)
51655-102-30	51655-102	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20140825	N/A	ANDA	ANDA075511	Northwind Pharmaceuticals	FAMOTIDINE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-102-30)
0172-5728-70	0172-5728	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075511	Teva Pharmaceuticals USA, Inc.	FAMOTIDINE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0172-5728-70)
0172-5729-70	0172-5729	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075511	Teva Pharmaceuticals USA, Inc.	FAMOTIDINE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0172-5729-70)
70518-0163-1	70518-0163	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20170202	N/A	ANDA	ANDA075511	REMEDYREPACK INC.	FAMOTIDINE	20 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0163-1)
0172-5728-80	0172-5728	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075511	Teva Pharmaceuticals USA, Inc.	FAMOTIDINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (0172-5728-80)
0172-5729-60	0172-5729	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075511	Teva Pharmaceuticals USA, Inc.	FAMOTIDINE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0172-5729-60)
0172-5728-60	0172-5728	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20010416	N/A	ANDA	ANDA075511	Teva Pharmaceuticals USA, Inc.	FAMOTIDINE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0172-5728-60)
68645-140-59	68645-140	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20091026	N/A	ANDA	ANDA075511	Legacy Pharmaceutical Packaging, LLC	FAMOTIDINE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68645-140-59)