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=ANDA206813"
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
42543-408-01 42543-408 HUMAN PRESCRIPTION DRUG POTASSIUM CITRATE EXTENDED RELEASE POTASSIUM CITRATE TABLET ORAL 20171101 N/A ANDA ANDA206813 Strides Pharma Inc. POTASSIUM CITRATE 15 meq/1 100 TABLET in 1 BOTTLE (42543-408-01)
42543-407-01 42543-407 HUMAN PRESCRIPTION DRUG POTASSIUM CITRATE EXTENDED RELEASE POTASSIUM CITRATE TABLET ORAL 20171101 N/A ANDA ANDA206813 Strides Pharma Inc. POTASSIUM CITRATE 10 meq/1 100 TABLET in 1 BOTTLE (42543-407-01)
42543-406-01 42543-406 HUMAN PRESCRIPTION DRUG POTASSIUM CITRATE EXTENDED RELEASE POTASSIUM CITRATE TABLET ORAL 20171101 N/A ANDA ANDA206813 Strides Pharma Inc. POTASSIUM CITRATE 5 meq/1 100 TABLET in 1 BOTTLE (42543-406-01)
71335-1706-1 71335-1706 HUMAN PRESCRIPTION DRUG POTASSIUM CITRATE EXTENDED RELEASE POTASSIUM CITRATE TABLET ORAL 20200910 N/A ANDA ANDA206813 Bryant Ranch Prepack POTASSIUM CITRATE 10 meq/1 30 TABLET in 1 BOTTLE (71335-1706-1)
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