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=ANDA218302"
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
42571-475-84 42571-475 HUMAN PRESCRIPTION DRUG Varenicline tartrate Varenicline tartrate KIT 20251201 N/A ANDA ANDA218302 Micro Labs Limited 1 KIT in 1 CARTON (42571-475-84) * 11 TABLET, FILM COATED in 1 BLISTER PACK * 42 TABLET, FILM COATED in 1 BLISTER PACK
42571-459-82 42571-459 HUMAN PRESCRIPTION DRUG varenicline tartrate varenicline tartrate TABLET, FILM COATED ORAL 20251201 N/A ANDA ANDA218302 Micro Labs Limited VARENICLINE TARTRATE .5 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (42571-459-82)
42571-460-82 42571-460 HUMAN PRESCRIPTION DRUG varenicline tartrate varenicline tartrate TABLET, FILM COATED ORAL 20251201 N/A ANDA ANDA218302 Micro Labs Limited VARENICLINE TARTRATE 1 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (42571-460-82)
42571-460-88 42571-460 HUMAN PRESCRIPTION DRUG varenicline tartrate varenicline tartrate TABLET, FILM COATED ORAL 20251201 N/A ANDA ANDA218302 Micro Labs Limited VARENICLINE TARTRATE 1 mg/1 1 BLISTER PACK in 1 CARTON (42571-460-88) / 56 TABLET, FILM COATED in 1 BLISTER PACK
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