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
16252-516-05	16252-516	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20061101	20260331	ANDA	ANDA076794	Teva Pharmaceuticals USA, Inc.	CIPROFLOXACIN HYDROCHLORIDE	750 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-516-05)
16252-515-01	16252-515	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20061101	20270831	ANDA	ANDA076794	Teva Pharmaceuticals USA, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-515-01)
16252-514-01	16252-514	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20061101	20260331	ANDA	ANDA076794	Teva Pharmaceuticals USA, Inc.	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-514-01)
42708-002-14	42708-002	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20180509	N/A	ANDA	ANDA076794	QPharma Inc	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-002-14)
68071-2267-1	68071-2267	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20200924	N/A	ANDA	ANDA076794	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2267-1)
68071-2269-4	68071-2269	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20200928	N/A	ANDA	ANDA076794	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2269-4)