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=NDA021537"
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
71205-309-75 71205-309 HUMAN PRESCRIPTION DRUG CIPRODEX ciprofloxacin and dexamethasone SUSPENSION/ DROPS AURICULAR (OTIC) 20190801 N/A NDA NDA021537 Proficient Rx LP CIPROFLOXACIN HYDROCHLORIDE; DEXAMETHASONE 3 mg/mL; 1 mg/mL 1 BOTTLE, DROPPER in 1 CARTON (71205-309-75) / 7.5 mL in 1 BOTTLE, DROPPER
63629-8797-1 63629-8797 HUMAN PRESCRIPTION DRUG Ciprofloxacin and Dexamethasone ciprofloxacin and dexamethasone SUSPENSION/ DROPS AURICULAR (OTIC) 20210910 N/A NDA AUTHORIZED GENERIC NDA021537 Bryant Ranch Prepack CIPROFLOXACIN HYDROCHLORIDE; DEXAMETHASONE 3 mg/mL; 1 mg/mL 1 BOTTLE, DROPPER in 1 CARTON (63629-8797-1) / 7.5 mL in 1 BOTTLE, DROPPER
0781-6186-67 0781-6186 HUMAN PRESCRIPTION DRUG Ciprofloxacin and Dexamethasone ciprofloxacin and dexamethasone SUSPENSION/ DROPS AURICULAR (OTIC) 20200810 N/A NDA AUTHORIZED GENERIC NDA021537 Sandoz Inc CIPROFLOXACIN HYDROCHLORIDE; DEXAMETHASONE 3 mg/mL; 1 mg/mL 1 BOTTLE, DROPPER in 1 CARTON (0781-6186-67) / 7.5 mL in 1 BOTTLE, DROPPER
0078-0799-75 0078-0799 HUMAN PRESCRIPTION DRUG CIPRODEX ciprofloxacin and dexamethasone SUSPENSION/ DROPS AURICULAR (OTIC) 20200728 N/A NDA NDA021537 Novartis Pharmaceuticals Corporation CIPROFLOXACIN HYDROCHLORIDE; DEXAMETHASONE 3 mg/mL; 1 mg/mL 1 BOTTLE in 1 CARTON (0078-0799-75) / 7.5 mL in 1 BOTTLE
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