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=ANDA212861"
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
70518-3525-0 70518-3525 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20220917 N/A ANDA ANDA212861 REMEDYREPACK INC. POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3525-0)
70518-3525-1 70518-3525 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230924 N/A ANDA ANDA212861 REMEDYREPACK INC. POTASSIUM CHLORIDE 750 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3525-1)
69238-1065-1 69238-1065 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20200511 N/A ANDA ANDA212861 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-1065-1)
69238-1065-7 69238-1065 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20200511 N/A ANDA ANDA212861 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-1065-7)
69238-1067-1 69238-1067 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20200511 N/A ANDA ANDA212861 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 1125 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-1067-1)
69238-1069-1 69238-1069 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20200511 N/A ANDA ANDA212861 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 1500 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-1069-1)
69238-1069-5 69238-1069 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20200511 N/A ANDA ANDA212861 Amneal Pharmaceuticals NY LLC POTASSIUM CHLORIDE 1500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-1069-5)
0904-7292-61 0904-7292 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230501 N/A ANDA ANDA212861 Major Pharmaceuticals POTASSIUM CHLORIDE 750 mg/1 100 BLISTER PACK in 1 CARTON (0904-7292-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0904-7293-61 0904-7293 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230501 N/A ANDA ANDA212861 Major Pharmaceuticals POTASSIUM CHLORIDE 1500 mg/1 100 BLISTER PACK in 1 CARTON (0904-7293-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
50090-5665-0 50090-5665 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210915 N/A ANDA ANDA212861 A-S Medication Solutions POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5665-0)
50090-5665-1 50090-5665 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210915 N/A ANDA ANDA212861 A-S Medication Solutions POTASSIUM CHLORIDE 1500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5665-1)
50090-5665-2 50090-5665 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20210915 N/A ANDA ANDA212861 A-S Medication Solutions POTASSIUM CHLORIDE 1500 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5665-2)
72789-239-30 72789-239 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20220324 N/A ANDA ANDA212861 PD-Rx Pharmaceuticals, Inc. POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-239-30)
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