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=ANDA216604"
符合检索条件的记录共 4 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
70121-1712-3 70121-1712 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride Dexmedetomidine Hydrochloride in Sodium Chloride INJECTION INTRAVENOUS 20230519 N/A ANDA ANDA216604 Amneal Pharmaceuticals LLC DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 12 POUCH in 1 CARTON (70121-1712-3) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
70121-1712-2 70121-1712 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride Dexmedetomidine Hydrochloride in Sodium Chloride INJECTION INTRAVENOUS 20240108 N/A ANDA ANDA216604 Amneal Pharmaceuticals LLC DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 10 POUCH in 1 CARTON (70121-1712-2) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
70121-1711-9 70121-1711 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride Dexmedetomidine Hydrochloride in Sodium Chloride INJECTION INTRAVENOUS 20230519 N/A ANDA ANDA216604 Amneal Pharmaceuticals LLC DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 24 POUCH in 1 CARTON (70121-1711-9) / 1 BAG in 1 POUCH / 50 mL in 1 BAG
70121-1711-2 70121-1711 HUMAN PRESCRIPTION DRUG Dexmedetomidine Hydrochloride Dexmedetomidine Hydrochloride in Sodium Chloride INJECTION INTRAVENOUS 20240108 N/A ANDA ANDA216604 Amneal Pharmaceuticals LLC DEXMEDETOMIDINE HYDROCHLORIDE 4 ug/mL 15 POUCH in 1 CARTON (70121-1711-2) / 1 BAG in 1 POUCH / 50 mL in 1 BAG
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