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=ANDA075604"
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
60687-756-09 60687-756 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240126 20261231 ANDA ANDA075604 American Health Packaging POTASSIUM CHLORIDE 20 meq/1 80 BLISTER PACK in 1 CARTON (60687-756-09) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-756-11)
62037-710-01 62037-710 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20020410 20260630 ANDA ANDA075604 Actavis Pharma, Inc. POTASSIUM CHLORIDE 10 meq/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-710-01)
82804-075-03 82804-075 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240212 N/A ANDA ANDA075604 Proficient Rx LP POTASSIUM CHLORIDE 20 meq/1 3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-03)
82804-075-06 82804-075 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240212 N/A ANDA ANDA075604 Proficient Rx LP POTASSIUM CHLORIDE 20 meq/1 6 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-06)
82804-075-10 82804-075 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240212 N/A ANDA ANDA075604 Proficient Rx LP POTASSIUM CHLORIDE 20 meq/1 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-10)
82804-075-30 82804-075 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240212 N/A ANDA ANDA075604 Proficient Rx LP POTASSIUM CHLORIDE 20 meq/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-30)
82804-075-60 82804-075 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240212 N/A ANDA ANDA075604 Proficient Rx LP POTASSIUM CHLORIDE 20 meq/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-60)
82804-075-90 82804-075 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20240212 N/A ANDA ANDA075604 Proficient Rx LP POTASSIUM CHLORIDE 20 meq/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-90)
62037-720-01 62037-720 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20020410 20270430 ANDA ANDA075604 Actavis Pharma, Inc. POTASSIUM CHLORIDE 20 meq/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-720-01)
62037-720-05 62037-720 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20020410 20260630 ANDA ANDA075604 Actavis Pharma, Inc. POTASSIUM CHLORIDE 20 meq/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-720-05)
62037-720-10 62037-720 HUMAN PRESCRIPTION DRUG Potassium Chloride Potassium Chloride TABLET, EXTENDED RELEASE ORAL 20020410 20261231 ANDA ANDA075604 Actavis Pharma, Inc. POTASSIUM CHLORIDE 20 meq/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-720-10)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase