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
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)
68001-566-00 68001-566 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET ORAL 20230417 N/A ANDA ANDA214452 Bluepoint Laboratories POTASSIUM CHLORIDE 750 mg/1 100 TABLET in 1 BOTTLE (68001-566-00)
68001-566-03 68001-566 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET ORAL 20230417 N/A ANDA ANDA214452 Bluepoint Laboratories POTASSIUM CHLORIDE 750 mg/1 500 TABLET in 1 BOTTLE (68001-566-03)
72189-648-04 72189-648 HUMAN PRESCRIPTION DRUG Potassium Chloride ER Potassium Chloride ER TABLET, EXTENDED RELEASE ORAL 20251104 N/A ANDA ANDA214452 Direct_Rx POTASSIUM CHLORIDE 750 mg/1 4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-04)
72189-648-30 72189-648 HUMAN PRESCRIPTION DRUG Potassium Chloride ER Potassium Chloride ER TABLET, EXTENDED RELEASE ORAL 20251104 N/A ANDA ANDA214452 Direct_Rx POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-30)
70518-4383-0 70518-4383 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20250702 N/A ANDA ANDA214452 REMEDYREPACK INC. POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4383-0)
70518-4383-1 70518-4383 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20250724 N/A ANDA ANDA214452 REMEDYREPACK INC. POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4383-1)
70010-135-01 70010-135 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20210130 N/A ANDA ANDA214452 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 1500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-135-01)
70010-135-05 70010-135 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20210130 N/A ANDA ANDA214452 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 1500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-135-05)
70010-135-10 70010-135 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20210130 N/A ANDA ANDA214452 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 1500 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-135-10)
68788-8196-3 68788-8196 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20220523 N/A ANDA ANDA214452 Preferred Pharmaceuticals Inc. POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-3)
68788-8196-6 68788-8196 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20220523 N/A ANDA ANDA214452 Preferred Pharmaceuticals Inc. POTASSIUM CHLORIDE 1500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-6)
68788-8196-9 68788-8196 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20220523 N/A ANDA ANDA214452 Preferred Pharmaceuticals Inc. POTASSIUM CHLORIDE 1500 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8196-9)
17856-1135-1 17856-1135 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20210130 N/A ANDA ANDA214452 Atlantic Biologicals Corp. POTASSIUM CHLORIDE 1500 mg/1 100 POUCH in 1 BOX, UNIT-DOSE (17856-1135-1) / 1 TABLET, EXTENDED RELEASE in 1 POUCH
70010-136-01 70010-136 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20210130 N/A ANDA ANDA214452 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-136-01)
70010-136-05 70010-136 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20210130 N/A ANDA ANDA214452 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-136-05)
70010-136-10 70010-136 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-release Potassium Chloride Extended-release TABLET, EXTENDED RELEASE ORAL 20210130 N/A ANDA ANDA214452 Granules Pharmaceuticals Inc. POTASSIUM CHLORIDE 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-136-10)
71335-2503-1 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 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-1)
71335-2503-2 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 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-2)
71335-2503-3 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 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase