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
71205-536-20	71205-536	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20210219	N/A	ANDA	ANDA077859	Proficient Rx LP	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71205-536-20)
71205-536-28	71205-536	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20210219	N/A	ANDA	ANDA077859	Proficient Rx LP	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71205-536-28)
71205-536-30	71205-536	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20210219	N/A	ANDA	ANDA077859	Proficient Rx LP	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-536-30)
71205-536-60	71205-536	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20210219	N/A	ANDA	ANDA077859	Proficient Rx LP	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-536-60)
71205-536-90	71205-536	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20210219	N/A	ANDA	ANDA077859	Proficient Rx LP	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-536-90)
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)
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)
70518-4214-0	70518-4214	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20241015	N/A	ANDA	ANDA077859	REMEDYREPACK INC.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-0)
70518-4214-1	70518-4214	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20241025	N/A	ANDA	ANDA077859	REMEDYREPACK INC.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)
70518-4214-2	70518-4214	HUMAN PRESCRIPTION DRUG	Ciprofloxacin	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20241113	N/A	ANDA	ANDA077859	REMEDYREPACK INC.	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	14 TABLET, FILM COATED in 1 BLISTER PACK (70518-4214-2)
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)
68071-4576-4	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	14 TABLET, FILM COATED in 1 BOTTLE (68071-4576-4)
68071-4576-6	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	60 TABLET, FILM COATED in 1 BOTTLE (68071-4576-6)