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
53002-2640-3	53002-2640	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171001	N/A	ANDA	ANDA076639	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	10 TABLET in 1 BOTTLE (53002-2640-3)
53002-2640-4	53002-2640	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171001	N/A	ANDA	ANDA076639	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET in 1 BOTTLE (53002-2640-4)
53002-2640-5	53002-2640	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171001	N/A	ANDA	ANDA076639	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	18 TABLET in 1 BOTTLE (53002-2640-5)
53002-2640-6	53002-2640	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171001	N/A	ANDA	ANDA076639	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET in 1 BOTTLE (53002-2640-6)
53002-2640-9	53002-2640	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171001	N/A	ANDA	ANDA076639	RPK Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	28 TABLET in 1 BOTTLE (53002-2640-9)
68071-4122-1	68071-4122	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171016	N/A	ANDA	ANDA076639	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	10 TABLET in 1 BOTTLE (68071-4122-1)
68071-4122-2	68071-4122	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171016	N/A	ANDA	ANDA076639	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET in 1 BOTTLE (68071-4122-2)
68071-4122-3	68071-4122	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171016	N/A	ANDA	ANDA076639	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET in 1 BOTTLE (68071-4122-3)
68071-4122-4	68071-4122	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171016	N/A	ANDA	ANDA076639	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET in 1 BOTTLE (68071-4122-4)
16571-413-05	16571-413	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20040910	N/A	ANDA	ANDA076639	Rising Pharma Holdings, Inc.	CIPROFLOXACIN HYDROCHLORIDE	750 mg/1	50 TABLET in 1 BOTTLE (16571-413-05)
68071-4122-6	68071-4122	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171016	N/A	ANDA	ANDA076639	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	60 TABLET in 1 BOTTLE (68071-4122-6)
68071-4122-7	68071-4122	HUMAN PRESCRIPTION DRUG	ciprofloxacin	ciprofloxacin	TABLET	ORAL	20171016	N/A	ANDA	ANDA076639	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	21 TABLET in 1 BOTTLE (68071-4122-7)