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=ANDA217151"
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
69315-403-56 69315-403 HUMAN PRESCRIPTION DRUG VARENICLINE TARTRATE VARENICLINE TARTRATE TABLET, FILM COATED ORAL 20231001 N/A ANDA ANDA217151 Leading Pharma, LLC VARENICLINE TARTRATE 1 mg/561 56 TABLET, FILM COATED in 1 BOTTLE (69315-403-56)
69315-403-58 69315-403 HUMAN PRESCRIPTION DRUG VARENICLINE TARTRATE VARENICLINE TARTRATE TABLET, FILM COATED ORAL 20231001 N/A ANDA ANDA217151 Leading Pharma, LLC VARENICLINE TARTRATE 1 mg/561 1 BLISTER PACK in 1 BOX (69315-403-58) / 56 TABLET, FILM COATED in 1 BLISTER PACK
69315-402-56 69315-402 HUMAN PRESCRIPTION DRUG VARENICLINE TARTRATE VARENICLINE TARTRATE TABLET, FILM COATED ORAL 20231001 N/A ANDA ANDA217151 Leading Pharma, LLC VARENICLINE TARTRATE .5 mg/561 56 TABLET, FILM COATED in 1 BOTTLE (69315-402-56)
69315-404-57 69315-404 HUMAN PRESCRIPTION DRUG VARENICLINE TARTRATE VARENICLINE TARTRATE KIT 20231001 N/A ANDA ANDA217151 Leading Pharma, LLC 1 KIT in 1 BOX (69315-404-57) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
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