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=ANDA214255"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
68462-893-56 68462-893 HUMAN PRESCRIPTION DRUG varenicline tartrate varenicline tartrate TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA214255 Glenmark Pharmaceuticals Inc., USA VARENICLINE TARTRATE .5 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (68462-893-56)
68462-894-04 68462-894 HUMAN PRESCRIPTION DRUG varenicline tartrate varenicline tartrate TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA214255 Glenmark Pharmaceuticals Inc., USA VARENICLINE TARTRATE 1 mg/1 1 BLISTER PACK in 1 CARTON (68462-894-04) / 56 TABLET, FILM COATED in 1 BLISTER PACK
68462-894-56 68462-894 HUMAN PRESCRIPTION DRUG varenicline tartrate varenicline tartrate TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA214255 Glenmark Pharmaceuticals Inc., USA VARENICLINE TARTRATE 1 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (68462-894-56)
68462-895-04 68462-895 HUMAN PRESCRIPTION DRUG varenicline tartrate varenicline tartrate KIT 20230822 N/A ANDA ANDA214255 Glenmark Pharmaceuticals Inc., USA 1 KIT in 1 CARTON (68462-895-04) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
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