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
69367-385-01	69367-385	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA076593	Westminster Pharmaceuticals, LLC	CIPROFLOXACIN HYDROCHLORIDE	250 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69367-385-01)
69367-387-50	69367-387	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA076593	Westminster Pharmaceuticals, LLC	CIPROFLOXACIN HYDROCHLORIDE	750 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (69367-387-50)
80425-0493-1	80425-0493	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20250320	N/A	ANDA	ANDA076593	Advanced Rx of Tennessee, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (80425-0493-1)
80425-0493-2	80425-0493	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20250320	N/A	ANDA	ANDA076593	Advanced Rx of Tennessee, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0493-2)
69367-386-01	69367-386	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA076593	Westminster Pharmaceuticals, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69367-386-01)
69367-386-05	69367-386	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20240523	N/A	ANDA	ANDA076593	Westminster Pharmaceuticals, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69367-386-05)
83939-0002-1	83939-0002	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20251103	N/A	ANDA	ANDA076593	VERITYRX, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	1 TABLET, FILM COATED in 1 POUCH (83939-0002-1)
83939-0002-2	83939-0002	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20251103	N/A	ANDA	ANDA076593	VERITYRX, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	50 POUCH in 1 BOX, UNIT-DOSE (83939-0002-2) / 1 TABLET, FILM COATED in 1 POUCH
83939-0002-3	83939-0002	HUMAN PRESCRIPTION DRUG	Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	TABLET, FILM COATED	ORAL	20251103	N/A	ANDA	ANDA076593	VERITYRX, LLC	CIPROFLOXACIN HYDROCHLORIDE	500 mg/1	100 POUCH in 1 BOX, UNIT-DOSE (83939-0002-3) / 1 TABLET, FILM COATED in 1 POUCH