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=ANDA073673"
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
0093-9222-05 0093-9222 HUMAN PRESCRIPTION DRUG Diflunisal Diflunisal TABLET, FILM COATED ORAL 20220825 N/A ANDA ANDA073673 Teva Pharmaceuticals USA, Inc. DIFLUNISAL 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (0093-9222-05)
0093-9222-06 0093-9222 HUMAN PRESCRIPTION DRUG Diflunisal Diflunisal TABLET, FILM COATED ORAL 20210630 N/A ANDA ANDA073673 Teva Pharmaceuticals USA, Inc. DIFLUNISAL 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (0093-9222-06)
0093-9222-01 0093-9222 HUMAN PRESCRIPTION DRUG Diflunisal Diflunisal TABLET, FILM COATED ORAL 20210630 N/A ANDA ANDA073673 Teva Pharmaceuticals USA, Inc. DIFLUNISAL 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0093-9222-01)
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