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
72189-141-90	72189-141	HUMAN PRESCRIPTION DRUG	FAMOTIDINE	FAMOTIDINE	TABLET	ORAL	20201015	N/A	ANDA	ANDA078916	direct rx	FAMOTIDINE	20 mg/1	90 TABLET in 1 BOTTLE (72189-141-90)
46708-293-30	46708-293	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160129	N/A	ANDA	ANDA078916	Alembic Pharmaceuticals Limited	FAMOTIDINE	20 mg/1	30 TABLET in 1 BOTTLE (46708-293-30)
46708-293-31	46708-293	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160129	N/A	ANDA	ANDA078916	Alembic Pharmaceuticals Limited	FAMOTIDINE	20 mg/1	100 TABLET in 1 BOTTLE (46708-293-31)
46708-293-71	46708-293	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160129	N/A	ANDA	ANDA078916	Alembic Pharmaceuticals Limited	FAMOTIDINE	20 mg/1	500 TABLET in 1 BOTTLE (46708-293-71)
46708-293-91	46708-293	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET	ORAL	20160129	N/A	ANDA	ANDA078916	Alembic Pharmaceuticals Limited	FAMOTIDINE	20 mg/1	1000 TABLET in 1 BOTTLE (46708-293-91)