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=ANDA208103"
符合检索条件的记录共 3 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
36000-262-05 36000-262 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride dexmedetomidine hydrochloride INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20260416 N/A ANDA ANDA208103 Baxter Healthcare Corporation DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 5 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-05) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01)
36000-262-10 36000-262 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride dexmedetomidine hydrochloride INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20260416 N/A ANDA ANDA208103 Baxter Healthcare Corporation DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-10) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01)
36000-262-25 36000-262 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride dexmedetomidine hydrochloride INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20260416 N/A ANDA ANDA208103 Baxter Healthcare Corporation DEXMEDETOMIDINE HYDROCHLORIDE 100 ug/mL 25 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-25) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01)
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