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=ANDA201785"
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
49884-156-76 49884-156 HUMAN PRESCRIPTION DRUG Varenicline varenicline tartrate TABLET, FILM COATED ORAL 20210921 N/A ANDA ANDA201785 ENDO USA, Inc. VARENICLINE TARTRATE 1 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (49884-156-76)
60687-648-21 60687-648 HUMAN PRESCRIPTION DRUG Varenicline varenicline tartrate TABLET, FILM COATED ORAL 20220211 N/A ANDA ANDA201785 American Health Packaging VARENICLINE TARTRATE 1 mg/1 30 BLISTER PACK in 1 CARTON (60687-648-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-648-11)
49884-155-76 49884-155 HUMAN PRESCRIPTION DRUG Varenicline varenicline tartrate TABLET, FILM COATED ORAL 20210921 N/A ANDA ANDA201785 ENDO USA, Inc. VARENICLINE TARTRATE .5 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (49884-155-76)
49884-944-99 49884-944 HUMAN PRESCRIPTION DRUG Varenicline varenicline tartrate KIT 20210921 N/A ANDA ANDA201785 ENDO USA, Inc. 1 KIT in 1 BOX (49884-944-99) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
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