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
68084-070-01	68084-070	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20040818	20250731	ANDA	ANDA076794	American Health Packaging	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-070-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-070-11)
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)
16252-514-01	16252-514	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20061101	N/A	ANDA	ANDA076794	Teva Pharmaceuticals USA, Inc.	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-514-01)
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)
16252-515-01	16252-515	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20061101	N/A	ANDA	ANDA076794	Teva Pharmaceuticals USA, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-515-01)
53002-2641-0	53002-2641	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA076794	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-2641-0)
53002-2641-1	53002-2641	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA076794	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	1 TABLET, FILM COATED in 1 BOTTLE (53002-2641-1)
53002-2641-2	53002-2641	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA076794	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (53002-2641-2)
53002-2641-3	53002-2641	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA076794	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (53002-2641-3)
53002-2641-4	53002-2641	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA076794	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (53002-2641-4)
53002-2641-5	53002-2641	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA076794	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	18 TABLET, FILM COATED in 1 BOTTLE (53002-2641-5)
53002-2641-6	53002-2641	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA076794	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (53002-2641-6)
53002-2641-9	53002-2641	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20220101	N/A	ANDA	ANDA076794	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (53002-2641-9)
16252-516-05	16252-516	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20061101	N/A	ANDA	ANDA076794	Teva Pharmaceuticals USA, Inc.	CIPROFLOXACIN HYDROCHLORIDE	750 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-516-05)