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
71335-2097-7	71335-2097	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, COATED	ORAL	20240403	N/A	ANDA	ANDA208921	Bryant Ranch Prepack	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	12 TABLET, COATED in 1 BOTTLE (71335-2097-7)
71335-2097-8	71335-2097	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, COATED	ORAL	20240403	N/A	ANDA	ANDA208921	Bryant Ranch Prepack	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	40 TABLET, COATED in 1 BOTTLE (71335-2097-8)
71335-2097-9	71335-2097	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, COATED	ORAL	20240403	N/A	ANDA	ANDA208921	Bryant Ranch Prepack	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	90 TABLET, COATED in 1 BOTTLE (71335-2097-9)
72189-623-10	72189-623	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET	ORAL	20250514	N/A	ANDA	ANDA208921	Direct_Rx	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	10 TABLET in 1 BOTTLE (72189-623-10)
72189-623-14	72189-623	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET	ORAL	20250514	N/A	ANDA	ANDA208921	Direct_Rx	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET in 1 BOTTLE (72189-623-14)
72189-623-20	72189-623	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET	ORAL	20250514	N/A	ANDA	ANDA208921	Direct_Rx	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET in 1 BOTTLE (72189-623-20)
67296-2169-1	67296-2169	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofolxacin	TABLET	ORAL	20231001	N/A	ANDA	ANDA208921	Redpharm Drug	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	10 TABLET in 1 BOTTLE (67296-2169-1)
67296-2169-6	67296-2169	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofolxacin	TABLET	ORAL	20231001	N/A	ANDA	ANDA208921	Redpharm Drug	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	6 TABLET in 1 BOTTLE (67296-2169-6)
67296-2169-7	67296-2169	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofolxacin	TABLET	ORAL	20231001	N/A	ANDA	ANDA208921	Redpharm Drug	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	14 TABLET in 1 BOTTLE (67296-2169-7)