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)
检索条件:" 注册申请号=ANDA075939"
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
69238-2433-1 69238-2433 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, FILM COATED ORAL 20240229 N/A ANDA ANDA075939 Amneal Pharmaceuticals NY LLC CIPROFLOXACIN HYDROCHLORIDE 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69238-2433-1)
69238-2434-1 69238-2434 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, FILM COATED ORAL 20240229 N/A ANDA ANDA075939 Amneal Pharmaceuticals NY LLC CIPROFLOXACIN HYDROCHLORIDE 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69238-2434-1)
69238-2434-5 69238-2434 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, FILM COATED ORAL 20240229 N/A ANDA ANDA075939 Amneal Pharmaceuticals NY LLC CIPROFLOXACIN HYDROCHLORIDE 750 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (69238-2434-5)
69238-2432-1 69238-2432 HUMAN PRESCRIPTION DRUG Ciprofloxacin Ciprofloxacin TABLET, FILM COATED ORAL 20240229 N/A ANDA ANDA075939 Amneal Pharmaceuticals NY LLC CIPROFLOXACIN HYDROCHLORIDE 250 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69238-2432-1)
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