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=ANDA212799"
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
69452-193-30 69452-193 HUMAN PRESCRIPTION DRUG Potassium Citrate Potassium Citrate TABLET, EXTENDED RELEASE ORAL 20191214 N/A ANDA ANDA212799 Bionpharma Inc. POTASSIUM CITRATE 10 meq/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-193-30)
69452-194-20 69452-194 HUMAN PRESCRIPTION DRUG Potassium Citrate Potassium Citrate TABLET, EXTENDED RELEASE ORAL 20191214 N/A ANDA ANDA212799 Bionpharma Inc. POTASSIUM CITRATE 15 meq/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-194-20)
69452-194-30 69452-194 HUMAN PRESCRIPTION DRUG Potassium Citrate Potassium Citrate TABLET, EXTENDED RELEASE ORAL 20191214 N/A ANDA ANDA212799 Bionpharma Inc. POTASSIUM CITRATE 15 meq/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-194-30)
69452-193-20 69452-193 HUMAN PRESCRIPTION DRUG Potassium Citrate Potassium Citrate TABLET, EXTENDED RELEASE ORAL 20191214 N/A ANDA ANDA212799 Bionpharma Inc. POTASSIUM CITRATE 10 meq/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69452-193-20)
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