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=ANDA214452"
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
71335-2503-4 71335-2503 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20240923 N/A ANDA ANDA214452 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-4)
72189-629-30 72189-629 HUMAN PRESCRIPTION DRUG Potassium Chloride ER Potassium Chloride ER TABLET, EXTENDED RELEASE ORAL 20250613 N/A ANDA ANDA214452 Direct_Rx POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-629-30)
71335-2503-5 71335-2503 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20240923 N/A ANDA ANDA214452 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-5)
71335-2503-6 71335-2503 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20240923 N/A ANDA ANDA214452 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-6)
71335-2503-7 71335-2503 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20240923 N/A ANDA ANDA214452 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-7)
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