Drug Registration and Acceptance

Drug Name

Exact

Active Ingredient

Acceptance No.

Manufacturers

Acceptance Date

Status Date

Classification

Review Status

Drug Type

Submission

Evaluation Conclusion

ATC Category

Special Approval Varieties

Task Type

Major Special Varieties

Sequence No.

Stock Code

Visualized Analysis Export Evaluation Conclusion Evaluation Progress

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