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
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)
71205-276-90	71205-276	HUMAN PRESCRIPTION DRUG	Famotidine	Famotidine	TABLET, FILM COATED	ORAL	20260313	N/A	ANDA	ANDA075511	Proficient Rx LP	FAMOTIDINE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-276-90)
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)
71205-276-30	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)
71205-276-60	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)