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
63187-129-60	63187-129	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20150401	N/A	ANDA	ANDA075805	Proficient Rx LP	FAMOTIDINE	20 mg/1	60 TABLET in 1 BOTTLE (63187-129-60)
63187-129-90	63187-129	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20150401	N/A	ANDA	ANDA075805	Proficient Rx LP	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE (63187-129-90)
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)
43063-695-95	43063-695	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20210222	N/A	ANDA	ANDA075805	PD-Rx Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (43063-695-95)
43063-696-30	43063-696	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160726	N/A	ANDA	ANDA075805	PD-Rx Pharmaceuticals, Inc.	FAMOTIDINE	40 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (43063-696-30)
43063-695-90	43063-695	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160726	N/A	ANDA	ANDA075805	PD-Rx Pharmaceuticals, Inc.	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (43063-695-90)