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
50090-3791-4	50090-3791	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA077859	A-S Medication Solutions	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3791-4)
42708-088-14	42708-088	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin	TABLET, FILM COATED	ORAL	20190111	20270228	ANDA	ANDA077859	QPharma Inc	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-088-14)
51655-216-53	51655-216	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230714	20270228	ANDA	ANDA077859	Northwind Health Company, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-53)
51655-216-84	51655-216	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230608	20270228	ANDA	ANDA077859	Northwind Health Company, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-84)
51655-216-87	51655-216	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230317	20270228	ANDA	ANDA077859	Northwind Health Company, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-87)
42708-188-14	42708-188	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20250131	N/A	ANDA	ANDA077859	QPharma, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-188-14)
51655-216-20	51655-216	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230628	20270228	ANDA	ANDA077859	Northwind Health Company, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-20)
51655-216-25	51655-216	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230818	20270228	ANDA	ANDA077859	Northwind Health Company, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-25)
51655-216-52	51655-216	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20240110	20270228	ANDA	ANDA077859	Northwind Health Company, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-216-52)
60687-860-01	60687-860	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20240930	20280229	ANDA	ANDA077859	American Health Packaging	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	100 BLISTER PACK in 1 CARTON (60687-860-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-860-11)
72189-111-14	72189-111	HUMAN PRESCRIPTION DRUG	CIPROFLOXACIN	ciprofloxacin hydrochloride	TABLET, FILM COATED	ORAL	20200612	N/A	ANDA	ANDA077859	DIRECT RX	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (72189-111-14)
82982-050-14	82982-050	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20230123	20260731	ANDA	ANDA077859	Pharmasource Meds, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (82982-050-14)
72189-111-20	72189-111	HUMAN PRESCRIPTION DRUG	CIPROFLOXACIN	ciprofloxacin hydrochloride	TABLET, FILM COATED	ORAL	20200612	N/A	ANDA	ANDA077859	DIRECT RX	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (72189-111-20)
72189-111-30	72189-111	HUMAN PRESCRIPTION DRUG	CIPROFLOXACIN	ciprofloxacin hydrochloride	TABLET, FILM COATED	ORAL	20200612	N/A	ANDA	ANDA077859	DIRECT RX	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30)
68071-3876-2	68071-3876	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20250724	N/A	ANDA	ANDA077859	NuCare Pharmaceuticals, Inc.	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (68071-3876-2)
76420-045-20	76420-045	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20200904	N/A	ANDA	ANDA077859	Asclemed USA, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (76420-045-20)
76420-045-30	76420-045	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20200904	N/A	ANDA	ANDA077859	Asclemed USA, Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-045-30)
68071-4576-1	68071-4576	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20180927	N/A	ANDA	ANDA077859	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (68071-4576-1)
68071-4576-2	68071-4576	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20180927	N/A	ANDA	ANDA077859	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-4576-2)
68071-4576-3	68071-4576	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20180927	N/A	ANDA	ANDA077859	NuCare Pharmaceuticals,Inc.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4576-3)