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
69367-387-50	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)
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)
69367-386-01	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)