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=ANDA209688"
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
50090-6639-0 50090-6639 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230829 N/A ANDA ANDA209688 A-S Medication Solutions POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-0)
50090-6639-1 50090-6639 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230829 N/A ANDA ANDA209688 A-S Medication Solutions POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-1)
50090-6639-2 50090-6639 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230829 N/A ANDA ANDA209688 A-S Medication Solutions POTASSIUM CHLORIDE 750 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-2)
50090-6639-3 50090-6639 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240112 N/A ANDA ANDA209688 A-S Medication Solutions POTASSIUM CHLORIDE 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6639-3)
71335-2447-1 71335-2447 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240918 N/A ANDA ANDA209688 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-1)
71335-2447-2 71335-2447 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240918 N/A ANDA ANDA209688 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-2)
71335-2447-3 71335-2447 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240918 N/A ANDA ANDA209688 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-3)
24979-231-01 24979-231 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230410 N/A ANDA ANDA209688 TWi Pharmaceuticals, Inc. POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-01)
24979-231-02 24979-231 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230410 N/A ANDA ANDA209688 TWi Pharmaceuticals, Inc. POTASSIUM CHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-02)
24979-231-03 24979-231 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20230410 N/A ANDA ANDA209688 TWi Pharmaceuticals, Inc. POTASSIUM CHLORIDE 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-03)
82804-057-30 82804-057 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240115 N/A ANDA ANDA209688 Proficient Rx LP POTASSIUM CHLORIDE 1500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-30)
82804-057-60 82804-057 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240115 N/A ANDA ANDA209688 Proficient Rx LP POTASSIUM CHLORIDE 1500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-60)
82804-057-90 82804-057 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240115 N/A ANDA ANDA209688 Proficient Rx LP POTASSIUM CHLORIDE 1500 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-90)
71335-2447-4 71335-2447 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240918 N/A ANDA ANDA209688 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-4)
71335-2447-5 71335-2447 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240918 N/A ANDA ANDA209688 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-5)
71335-2447-6 71335-2447 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240918 N/A ANDA ANDA209688 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-6)
71335-2447-7 71335-2447 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240918 N/A ANDA ANDA209688 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2447-7)
69680-133-00 69680-133 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20200701 N/A ANDA ANDA209688 Vitruvias Therapeutics POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69680-133-00)
69680-133-92 69680-133 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20200731 N/A ANDA ANDA209688 Vitruvias Therapeutics POTASSIUM CHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69680-133-92)
69680-133-93 69680-133 HUMAN PRESCRIPTION DRUG Potassium Chloride Extended-Release Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20200701 N/A ANDA ANDA209688 Vitruvias Therapeutics POTASSIUM CHLORIDE 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69680-133-93)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase