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=NDA020936"
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
60505-1318-3 60505-1318 HUMAN PRESCRIPTION DRUG PAROXETINE HYDROCHLORIDE paroxetine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190809 N/A NDA NDA020936 Apotex Corp PAROXETINE HYDROCHLORIDE HEMIHYDRATE 37.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1318-3)
60505-4378-3 60505-4378 HUMAN PRESCRIPTION DRUG PAXIL CR paroxetine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110101 N/A NDA NDA020936 Apotex Corp PAROXETINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-4378-3)
60505-4379-3 60505-4379 HUMAN PRESCRIPTION DRUG PAXIL CR paroxetine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110101 N/A NDA NDA020936 Apotex Corp PAROXETINE HYDROCHLORIDE 37.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-4379-3)
60505-1317-3 60505-1317 HUMAN PRESCRIPTION DRUG PAROXETINE HYDROCHLORIDE paroxetine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190809 N/A NDA NDA020936 Apotex Corp PAROXETINE HYDROCHLORIDE HEMIHYDRATE 25 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1317-3)
60505-1316-3 60505-1316 HUMAN PRESCRIPTION DRUG PAROXETINE HYDROCHLORIDE paroxetine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20190809 N/A NDA NDA020936 Apotex Corp PAROXETINE HYDROCHLORIDE 12.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1316-3)
60505-4377-3 60505-4377 HUMAN PRESCRIPTION DRUG PAXIL CR paroxetine hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20110101 N/A NDA NDA020936 Apotex Corp PAROXETINE HYDROCHLORIDE 12.5 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-4377-3)
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