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
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)
76420-045-14	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	14 TABLET, FILM COATED in 1 BOTTLE (76420-045-14)
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)
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)
76420-045-10	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	10 TABLET, FILM COATED in 1 BOTTLE (76420-045-10)