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Acceptance No. Drug Name Active Ingredient Dosage Form Classification Submission Acceptance Date Manufacturers Manufacturers Review Status Status Date View
JXHL0800340 格列美脲马来酸罗格列酮片(I) glimepiride;rosiglitazone maleate Tablet Chemical Drugs Import Drug Application 2008-10-29 GlaxoSmithKline Inc. Glaxosmithkline Inc Certificate Issued 2010-04-14 view
JXHL0800341 格列美脲马来酸罗格列酮片(II) glimepiride;rosiglitazone maleate Tablet Chemical Drugs Import Drug Application 2008-10-17 GlaxoSmithKline Inc. Glaxosmithkline Inc Certificate Issued 2010-04-14 view
JXHL0800342 格列美脲马来酸罗格列酮片(III) glimepiride;rosiglitazone maleate Tablet Chemical Drugs Import Drug Application 2008-10-17 GlaxoSmithKline Inc. Glaxosmithkline Inc Certificate Issued 2010-04-14 view
JXHS0800070 盐酸帕罗西汀控释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Import Drug Application 2008-12-25 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2010-08-18 view
JXHS0800071 盐酸帕罗西汀控释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Import Drug Application 2008-12-25 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2010-08-18 view
JYHB1400499 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2014-04-17 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2014-10-21 view
JYHB1701477 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2017-12-08 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2018-04-10 view
JYHB1100106 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2011-02-21 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2012-04-09 view
JYHB1501094 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2015-08-14 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2016-11-24 view
JYHB1701478 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2017-12-08 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2018-04-10 view
JYHB1100105 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2011-02-21 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2012-04-09 view
JYHB1501096 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2015-08-14 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2016-11-24 view
JYHB1400498 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2014-04-17 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2014-10-21 view
JYHZ1600112 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs License Renew 2016-05-12 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2017-02-04 view
JXHL0900424 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Import Drug Application 2010-01-04 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2011-06-15 view
JXHL1400317 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Import Drug Application 2014-10-08 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2016-03-28 view
JYHB1100108 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2011-03-17 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2011-07-29 view
JXHL0900423 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Import Drug Application 2009-12-24 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2011-06-15 view
JXHL1400318 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Import Drug Application 2014-09-28 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2016-03-28 view
JYHB1100107 盐酸帕罗西汀肠溶缓释片 paroxetine hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2011-03-17 GLAXOSMITHKLINE INC. Glaxosmithkline Inc Certificate Issued 2011-07-29 view