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
68001-445-03 68001-445 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20201002 20241031 ANDA ANDA203562 BluePoint Laboratories POTASSIUM CHLORIDE 1500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-445-03)
68001-445-00 68001-445 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20201002 20241031 ANDA ANDA203562 BluePoint Laboratories POTASSIUM CHLORIDE 1500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-445-00)
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)
67296-1437-2 67296-1437 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20160726 N/A ANDA ANDA203562 Redpharm Drug, Inc. POTASSIUM CHLORIDE 1500 mg/1 2 TABLET, EXTENDED RELEASE in 1 BOTTLE (67296-1437-2)
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)
68462-471-01 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/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-471-01)
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)
71335-1781-3 71335-1781 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20210309 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-3)
71335-1781-4 71335-1781 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20211220 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-4)
71335-1781-5 71335-1781 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20211220 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-5)
71335-1781-6 71335-1781 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20211220 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-6)
71335-1781-7 71335-1781 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20210308 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-7)
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)
71335-1781-1 71335-1781 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20210526 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-1)
71335-1781-2 71335-1781 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20210625 N/A ANDA ANDA203562 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1781-2)
68001-367-00 68001-367 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20180630 20241031 ANDA ANDA203562 BluePoint Laboratories POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-367-00)
68001-367-03 68001-367 HUMAN PRESCRIPTION DRUG potassium chloride potassium chloride TABLET, EXTENDED RELEASE ORAL 20180630 20241031 ANDA ANDA203562 BluePoint Laboratories POTASSIUM CHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-367-03)
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