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=ANDA205993"
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
0574-0275-11 0574-0275 HUMAN PRESCRIPTION DRUG Potassium chloride extended release Potassium chloride TABLET, EXTENDED RELEASE ORAL 20160505 N/A ANDA ANDA205993 Padagis US LLC POTASSIUM CHLORIDE 750 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0574-0275-11) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
55154-6709-0 55154-6709 HUMAN PRESCRIPTION DRUG Potassium chloride extended release Potassium chloride TABLET, EXTENDED RELEASE ORAL 20160505 N/A ANDA ANDA205993 Cardinal Health 107, LLC POTASSIUM CHLORIDE 10 meq/1 10 BLISTER PACK in 1 BAG (55154-6709-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
63629-8442-1 63629-8442 HUMAN PRESCRIPTION DRUG Potassium chloride extended release Potassium chloride TABLET, EXTENDED RELEASE ORAL 20151218 N/A ANDA ANDA205993 Bryant Ranch Prepack POTASSIUM CHLORIDE 750 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8442-1)
63629-8443-1 63629-8443 HUMAN PRESCRIPTION DRUG Potassium chloride extended release Potassium chloride TABLET, EXTENDED RELEASE ORAL 20160106 N/A ANDA ANDA205993 Bryant Ranch Prepack POTASSIUM CHLORIDE 600 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8443-1)
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