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=ANDA203562"
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
72189-462-30 72189-462 HUMAN PRESCRIPTION DRUG Potassium Chloride ER Potassium Chloride ER TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA203562 Direct_Rx POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-462-30)
68462-471-05 68462-471 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20160726 N/A ANDA ANDA203562 Glenmark Pharmaceuticals Inc., USA POTASSIUM CHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-471-05)
68462-472-01 68462-472 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20160726 N/A ANDA ANDA203562 Glenmark Pharmaceuticals Inc., USA POTASSIUM CHLORIDE 1500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-01)
68462-472-05 68462-472 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20160726 N/A ANDA ANDA203562 Glenmark Pharmaceuticals Inc., USA POTASSIUM CHLORIDE 1500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-05)
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