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=ANDA210041"
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
50268-674-15 50268-674 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride SOLUTION ORAL 20230126 N/A ANDA ANDA210041 AvPAK POTASSIUM CHLORIDE 1.5 g/15mL 50 CUP in 1 BOX (50268-674-15) / 15 mL in 1 CUP (50268-674-11)
69238-1459-4 69238-1459 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride SOLUTION ORAL 20180724 N/A ANDA ANDA210041 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 1.5 g/15mL 10 CUP, UNIT-DOSE in 1 TRAY (69238-1459-4) / 15 mL in 1 CUP, UNIT-DOSE (69238-1459-3)
69238-1459-2 69238-1459 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride SOLUTION ORAL 20180724 N/A ANDA ANDA210041 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 1.5 g/15mL 473 mL in 1 BOTTLE (69238-1459-2)
17856-1458-1 17856-1458 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride SOLUTION ORAL 20230920 N/A ANDA ANDA210041 ATLANTIC BIOLOGICALS CORP. POTASSIUM CHLORIDE 3 g/15mL 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1458-1) / 15 mL in 1 CUP, UNIT-DOSE (17856-1458-2)
50268-675-12 50268-675 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride SOLUTION ORAL 20230126 N/A ANDA ANDA210041 AvPAK POTASSIUM CHLORIDE 3 g/15mL 20 CUP in 1 BOX (50268-675-12) / 15 mL in 1 CUP (50268-675-11)
69238-1458-2 69238-1458 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride SOLUTION ORAL 20180724 N/A ANDA ANDA210041 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 3 g/15mL 473 mL in 1 BOTTLE (69238-1458-2)
69238-1458-4 69238-1458 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride SOLUTION ORAL 20180724 N/A ANDA ANDA210041 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 3 g/15mL 10 CUP, UNIT-DOSE in 1 TRAY (69238-1458-4) / 15 mL in 1 CUP, UNIT-DOSE (69238-1458-3)
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