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=ANDA203129"
符合检索条件的记录共 2 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
76045-210-10 76045-210 HUMAN PRESCRIPTION DRUG Dexamethasone Sodium Phosphate Dexamethasone Sodium Phosphate INJECTION, SOLUTION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE 20201130 N/A ANDA ANDA203129 Fresenius Kabi USA, LLC DEXAMETHASONE SODIUM PHOSPHATE 4 mg/mL 24 BLISTER PACK in 1 CARTON (76045-210-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-210-00) / 1 mL in 1 SYRINGE, GLASS
76045-106-10 76045-106 HUMAN PRESCRIPTION DRUG Dexamethasone Sodium Phosphate Dexamethasone Sodium Phosphate INJECTION, SOLUTION INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE 20151030 N/A ANDA ANDA203129 Fresenius Kabi USA, LLC DEXAMETHASONE SODIUM PHOSPHATE 4 mg/mL 24 BLISTER PACK in 1 CARTON (76045-106-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASS
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