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
80425-0164-1	80425-0164	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20040609	N/A	ANDA	ANDA075593	Advanced Rx Pharmacy of Tennessee, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (80425-0164-1)
80425-0164-2	80425-0164	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20040609	N/A	ANDA	ANDA075593	Advanced Rx Pharmacy of Tennessee, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0164-2)
72189-242-10	72189-242	HUMAN PRESCRIPTION DRUG	CIPROFLOXACIN	CIPROFLOXACIN	TABLET, FILM COATED	ORAL	20210723	N/A	ANDA	ANDA075593	direct rx	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (72189-242-10)
72189-242-20	72189-242	HUMAN PRESCRIPTION DRUG	CIPROFLOXACIN	CIPROFLOXACIN	TABLET, FILM COATED	ORAL	20210723	N/A	ANDA	ANDA075593	direct rx	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (72189-242-20)