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=ANDA215371"
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
65219-389-05 65219-389 HUMAN PRESCRIPTION DRUG Multiple Electrolytes pH 7.4 sodium chloride, sodium gluconate, sodium acetate, potassium chloride and magnesium chloride INJECTION, SOLUTION INTRAVENOUS 20221021 N/A ANDA ANDA215371 Fresenius Kabi USA, LLC MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE 30 mg/100mL; 37 mg/100mL; 368 mg/100mL; 526 mg/100mL; 502 mg/100mL 20 BAG in 1 CASE (65219-389-05) / 500 mL in 1 BAG (65219-389-00)
65219-389-10 65219-389 HUMAN PRESCRIPTION DRUG Multiple Electrolytes pH 7.4 sodium chloride, sodium gluconate, sodium acetate, potassium chloride and magnesium chloride INJECTION, SOLUTION INTRAVENOUS 20221021 N/A ANDA ANDA215371 Fresenius Kabi USA, LLC MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE 30 mg/100mL; 37 mg/100mL; 368 mg/100mL; 526 mg/100mL; 502 mg/100mL 10 BAG in 1 CASE (65219-389-10) / 1000 mL in 1 BAG (65219-389-02)
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