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=ANDA211862"
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
70748-125-13 70748-125 HUMAN PRESCRIPTION DRUG VARENICLINE TARTRATE VARENICLINE TARTRATE KIT 20240320 N/A ANDA ANDA211862 Lupin Pharmaceuticals, Inc. 1 BLISTER PACK in 1 CARTON (70748-125-13) / 1 KIT in 1 BLISTER PACK
70748-126-13 70748-126 HUMAN PRESCRIPTION DRUG VARENICLINE VARENICLINE TABLET, FILM COATED ORAL 20240216 N/A ANDA ANDA211862 Lupin Pharmaceuticals, Inc. VARENICLINE TARTRATE 1 mg/1 1 BLISTER PACK in 1 CARTON (70748-126-13) / 56 TABLET, FILM COATED in 1 BLISTER PACK
70748-128-49 70748-128 HUMAN PRESCRIPTION DRUG VARENICLINE VARENICLINE TABLET, FILM COATED ORAL 20240109 N/A ANDA ANDA211862 Lupin Pharmaceuticals, Inc. VARENICLINE TARTRATE 1 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (70748-128-49)
70748-127-49 70748-127 HUMAN PRESCRIPTION DRUG VARENICLINE VARENICLINE TABLET, FILM COATED ORAL 20240109 N/A ANDA ANDA211862 Lupin Pharmaceuticals, Inc. VARENICLINE TARTRATE .5 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (70748-127-49)
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