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=ANDA210332"
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
65219-243-50 65219-243 HUMAN PRESCRIPTION DRUG Lactated Ringers and Dextrose SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE INJECTION, SOLUTION INTRAVENOUS 20221222 N/A ANDA ANDA210332 Fresenius Kabi USA, LLC CALCIUM CHLORIDE; DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE 20 mg/100mL; 5 g/100mL; 30 mg/100mL; 600 mg/100mL; 310 mg/100mL 20 BAG in 1 CASE (65219-243-50) / 500 mL in 1 BAG (65219-243-01)
65219-241-10 65219-241 HUMAN PRESCRIPTION DRUG Lactated Ringers and Dextrose SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE INJECTION, SOLUTION INTRAVENOUS 20220328 N/A ANDA ANDA210332 Fresenius Kabi USA, LLC CALCIUM CHLORIDE; DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE 20 mg/100mL; 5 g/100mL; 30 mg/100mL; 600 mg/100mL; 310 mg/100mL 10 BAG in 1 CASE (65219-241-10) / 1000 mL in 1 BAG (65219-241-00)
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