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=ANDA209192"
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
76045-109-10 76045-109 HUMAN PRESCRIPTION DRUG Dexamethasone Sodium Phosphate DEXAMETHASONE SODIUM PHOSPHATE INJECTION, EMULSION INTRAMUSCULAR; INTRAVENOUS 20180706 N/A ANDA ANDA209192 Fresenius Kabi USA, LLC DEXAMETHASONE SODIUM PHOSPHATE 10 mg/mL 24 BLISTER PACK in 1 CARTON (76045-109-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASS (76045-109-01)
76045-212-10 76045-212 HUMAN PRESCRIPTION DRUG Dexamethasone Sodium Phosphate DEXAMETHASONE SODIUM PHOSPHATE INJECTION, EMULSION INTRAMUSCULAR; INTRAVENOUS 20240221 N/A ANDA ANDA209192 Fresenius Kabi USA, LLC DEXAMETHASONE SODIUM PHOSPHATE 10 mg/mL 24 BLISTER PACK in 1 CARTON (76045-212-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASS (76045-212-00)
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