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=ANDA213647"
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
69238-1678-1 69238-1678 HUMAN PRESCRIPTION DRUG fluphenazine hydrochloride fluphenazine hydrochloride TABLET, FILM COATED ORAL 20200711 N/A ANDA ANDA213647 Amneal Pharmaceuticals NY LLC FLUPHENAZINE HYDROCHLORIDE 1 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1678-1)
69238-1679-1 69238-1679 HUMAN PRESCRIPTION DRUG fluphenazine hydrochloride fluphenazine hydrochloride TABLET, FILM COATED ORAL 20200711 N/A ANDA ANDA213647 Amneal Pharmaceuticals NY LLC FLUPHENAZINE HYDROCHLORIDE 2.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1679-1)
69238-1680-1 69238-1680 HUMAN PRESCRIPTION DRUG fluphenazine hydrochloride fluphenazine hydrochloride TABLET, FILM COATED ORAL 20200711 N/A ANDA ANDA213647 Amneal Pharmaceuticals NY LLC FLUPHENAZINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1680-1)
69238-1681-1 69238-1681 HUMAN PRESCRIPTION DRUG fluphenazine hydrochloride fluphenazine hydrochloride TABLET, FILM COATED ORAL 20200711 N/A ANDA ANDA213647 Amneal Pharmaceuticals NY LLC FLUPHENAZINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69238-1681-1)
70518-3569-0 70518-3569 HUMAN PRESCRIPTION DRUG fluphenazine hydrochloride fluphenazine hydrochloride TABLET, FILM COATED ORAL 20221102 N/A ANDA ANDA213647 REMEDYREPACK INC. FLUPHENAZINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3569-0)
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