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=ANDA076968"
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
69584-674-90 69584-674 HUMAN PRESCRIPTION DRUG paroxetine hydrochloride paroxetine hydrochloride TABLET, FILM COATED ORAL 20221114 N/A ANDA ANDA076968 Oxford Pharmaceuticals, LLC PAROXETINE HYDROCHLORIDE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69584-674-90)
69584-671-09 69584-671 HUMAN PRESCRIPTION DRUG paroxetine hydrochloride paroxetine hydrochloride TABLET, FILM COATED ORAL 20221114 N/A ANDA ANDA076968 Oxford Pharmaceuticals, LLC PAROXETINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (69584-671-09)
69584-671-10 69584-671 HUMAN PRESCRIPTION DRUG paroxetine hydrochloride paroxetine hydrochloride TABLET, FILM COATED ORAL 20221114 N/A ANDA ANDA076968 Oxford Pharmaceuticals, LLC PAROXETINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69584-671-10)
69584-671-50 69584-671 HUMAN PRESCRIPTION DRUG paroxetine hydrochloride paroxetine hydrochloride TABLET, FILM COATED ORAL 20221114 N/A ANDA ANDA076968 Oxford Pharmaceuticals, LLC PAROXETINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (69584-671-50)
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