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=ANDA202902"
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
68382-529-60 68382-529 HUMAN PRESCRIPTION DRUG CHOLESTYRAMINE CHOLESTYRAMINE POWDER, FOR SUSPENSION ORAL 20170608 N/A ANDA ANDA202902 Zydus Pharmaceuticals (USA) Inc. CHOLESTYRAMINE 4 g/5.5g 60 POUCH in 1 CARTON (68382-529-60) / 5.5 g in 1 POUCH
68382-529-42 68382-529 HUMAN PRESCRIPTION DRUG CHOLESTYRAMINE CHOLESTYRAMINE POWDER, FOR SUSPENSION ORAL 20170608 N/A ANDA ANDA202902 Zydus Pharmaceuticals (USA) Inc. CHOLESTYRAMINE 4 g/5.5g 231 g in 1 CONTAINER (68382-529-42)
70771-1070-2 70771-1070 HUMAN PRESCRIPTION DRUG CHOLESTYRAMINE CHOLESTYRAMINE POWDER, FOR SUSPENSION ORAL 20170608 N/A ANDA ANDA202902 Zydus Lifesciences Limited CHOLESTYRAMINE 4 g/5.5g 60 POUCH in 1 CARTON (70771-1070-2) / 5.5 g in 1 POUCH
70771-1070-1 70771-1070 HUMAN PRESCRIPTION DRUG CHOLESTYRAMINE CHOLESTYRAMINE POWDER, FOR SUSPENSION ORAL 20170608 N/A ANDA ANDA202902 Zydus Lifesciences Limited CHOLESTYRAMINE 4 g/5.5g 231 g in 1 CONTAINER (70771-1070-1)
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