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=ANDA216792"
符合检索条件的记录共 2 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
70677-1315-1 70677-1315 HUMAN OTC DRUG FOSTER AND THRIVE ALLERGY AND CONGESTION D fexofenadine hydrochloride, pseudoephedrine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260211 N/A ANDA ANDA216792 Strategic Sourcing Services LLC FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 20 BLISTER PACK in 1 CARTON (70677-1315-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
70677-1315-2 70677-1315 HUMAN OTC DRUG FOSTER AND THRIVE ALLERGY AND CONGESTION D fexofenadine hydrochloride, pseudoephedrine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260211 N/A ANDA ANDA216792 Strategic Sourcing Services LLC FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 30 BLISTER PACK in 1 CARTON (70677-1315-2) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase