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
CXS95401	盐酸普萘洛尔缓释片	propranolol hydrochloride	Tablet, extended release	Chemical Drugs	New Drug Application	2000-01-01			Certificate Issued	2009-10-21	view
CYHS0890157	盐酸普萘洛尔缓释片	propranolol hydrochloride	Tablet, extended release	Chemical Drugs(6)	Generic Drug	2008-08-01	山西亚宝药业集团股份有限公司	Yabao Pharmaceutical Group Co Ltd	Certificate Issued	2010-08-18	view
CYHS0509147	盐酸普萘洛尔缓释片	propranolol hydrochloride	Tablet, extended release	Chemical Drugs(6)	Generic Drug	2006-02-07	山西亚宝药业集团股份有限公司	Yabao Pharmaceutical Group Co Ltd	Certificate Issued	2006-12-13	view
CYHR1600014	盐酸普萘洛尔缓释片	propranolol hydrochloride	Tablet, extended release	Chemical Drugs	State Standards	2016-02-18	山西振东制药股份有限公司	Shanxi Zhendong Pharmaceutical Co Ltd	Certificate Issued	2016-12-08	view
CYHS1301175	盐酸普萘洛尔缓释片	propranolol hydrochloride	Tablet, extended release	Chemical Drugs(6)	Generic Drug	2014-12-09	山西振东制药股份有限公司	Shanxi Zhendong Pharmaceutical Co Ltd	Certificate Issued	2015-12-24	view