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=ANDA203854"
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
68788-8829-8 68788-8829 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20250213 N/A ANDA ANDA203854 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-8829-8)
68788-8829-1 68788-8829 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20250213 N/A ANDA ANDA203854 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8829-1)
68788-8829-3 68788-8829 HUMAN PRESCRIPTION DRUG Paroxetine paroxetine hydrochloride hemihydrate TABLET, FILM COATED ORAL 20250213 N/A ANDA ANDA203854 Preferred Pharmaceuticals Inc. PAROXETINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8829-3)
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