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=NDA203195"
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
68180-423-08 68180-423 HUMAN PRESCRIPTION DRUG CEFIXIME CEFIXIME CAPSULE ORAL 20201014 N/A NDA AUTHORIZED GENERIC NDA203195 Lupin Pharmaceuticals, Inc. CEFIXIME 400 mg/1 50 CAPSULE in 1 BOTTLE (68180-423-08)
68180-423-11 68180-423 HUMAN PRESCRIPTION DRUG CEFIXIME CEFIXIME CAPSULE ORAL 20201014 N/A NDA AUTHORIZED GENERIC NDA203195 Lupin Pharmaceuticals, Inc. CEFIXIME 400 mg/1 1 BLISTER PACK in 1 CARTON (68180-423-11) / 10 CAPSULE in 1 BLISTER PACK
70518-3221-0 70518-3221 HUMAN PRESCRIPTION DRUG CEFIXIME CEFIXIME CAPSULE ORAL 20210914 N/A NDA AUTHORIZED GENERIC NDA203195 REMEDYREPACK INC. CEFIXIME 400 mg/1 2 POUCH in 1 BOX (70518-3221-0) / 1 CAPSULE in 1 POUCH (70518-3221-1)
70518-3221-2 70518-3221 HUMAN PRESCRIPTION DRUG CEFIXIME CEFIXIME CAPSULE ORAL 20211104 N/A NDA AUTHORIZED GENERIC NDA203195 REMEDYREPACK INC. CEFIXIME 400 mg/1 2 POUCH in 1 BOX (70518-3221-2) / 1 CAPSULE in 1 POUCH (70518-3221-3)
70518-3221-4 70518-3221 HUMAN PRESCRIPTION DRUG CEFIXIME CEFIXIME CAPSULE ORAL 20220302 N/A NDA AUTHORIZED GENERIC NDA203195 REMEDYREPACK INC. CEFIXIME 400 mg/1 2 CAPSULE in 1 BOTTLE, PLASTIC (70518-3221-4)
70518-3221-5 70518-3221 HUMAN PRESCRIPTION DRUG CEFIXIME CEFIXIME CAPSULE ORAL 20220606 N/A NDA AUTHORIZED GENERIC NDA203195 REMEDYREPACK INC. CEFIXIME 400 mg/1 2 CAPSULE in 1 BOTTLE, PLASTIC (70518-3221-5)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase