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Acceptance No. Drug Name Active Ingredient Dosage Form Classification Submission Acceptance Date Manufacturers Manufacturers Review Status Status Date 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
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
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
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
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
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
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
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