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Acceptance No. Drug Name Active Ingredient Dosage Form Classification Submission Acceptance Date Manufacturers Manufacturers Review Status Status Date View
JXHS1100013 丁丙诺啡透皮贴剂 buprenorphine Patch Chemical Drugs Import Drug Application 2011-02-22 Mundipharma GmbH Mundipharma GmbH Certificate Issued 2013-01-09 view
JXHS1100015 丁丙诺啡透皮贴剂 buprenorphine Patch Chemical Drugs Import Drug Application 2011-02-22 Mundipharma GmbH Mundipharma GmbH Certificate Issued 2013-01-09 view
JXHS1100014 丁丙诺啡透皮贴剂 buprenorphine Patch Chemical Drugs Import Drug Application 2011-02-22 Mundipharma GmbH Mundipharma GmbH Certificate Issued 2013-01-09 view
JXHL0700099 丁丙诺啡透皮贴剂 buprenorphine Patch Chemical Drugs(3.1) Import Drug Application 2007-05-11 Mundipharma GmbH Mundipharma GmbH Certificate Issued 2008-11-27 view
JXHL0600161 盐酸曲马多缓释片 tramadol hydrochloride Tablet, extended release Chemical Drugs(3.1) Import Drug Application 2006-06-09 MUNDIPHARMA GmbH Mundipharma GmbH Certificate Issued 2007-06-04 view
JYHZ1200005 盐酸曲马多缓释片 tramadol hydrochloride Tablet, extended release Chemical Drugs License Renew 2012-02-22 MUNDIPHARMA GmbH Mundipharma GmbH Certificate Issued 2012-09-18 view
JYHZ1200006 盐酸曲马多缓释片 tramadol hydrochloride Tablet, extended release Chemical Drugs License Renew 2012-02-13 MUNDIPHARMA GmbH Mundipharma GmbH Certificate Issued 2012-09-18 view
JYHB1700593 盐酸曲马多缓释片 tramadol hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2017-05-19 MUNDIPHARMA GmbH Mundipharma GmbH Certificate Issued 2020-06-17 view
JYHB1700594 盐酸曲马多缓释片 tramadol hydrochloride Tablet, extended release Chemical Drugs Supplementary Application 2017-04-25 MUNDIPHARMA GmbH Mundipharma GmbH Certificate Issued 2020-06-17 view
JXHL0900146 羟考酮纳洛酮缓释片 naloxone hydrochloride;oxycodone hydrochloride Tablet, extended release Chemical Drugs Import Drug Application 2009-05-06 Mundipharma GmbH Mundipharma GmbH Certificate Issued 2011-07-04 view
JXHL0900145 羟考酮纳洛酮缓释片 naloxone hydrochloride;oxycodone hydrochloride Tablet, extended release Chemical Drugs Import Drug Application 2009-05-06 Mundipharma GmbH Mundipharma GmbH Certificate Issued 2011-07-04 view