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
CXHB1300021	盐酸雷诺嗪缓释片	Ranolazine hydrochloride	Tablet, extended release	Chemical Drugs	Supplementary Application	2013-07-23	齐鲁制药有限公司	QILU Pharmaceutical Co Ltd	Certificate Issued	2015-01-07	view
CXHL0500985	盐酸雷诺嗪缓释片	Ranolazine hydrochloride	Tablet, extended release	Chemical Drugs(1.1)	New Drug Application	2005-06-15	齐鲁制药有限公司	QILU Pharmaceutical Co Ltd	Certificate Issued	2005-10-18	view
CXHL0500984	盐酸雷诺嗪缓释片	Ranolazine hydrochloride	Tablet, extended release	Chemical Drugs(1.1)	New Drug Application	2005-06-15	齐鲁制药有限公司	QILU Pharmaceutical Co Ltd	Certificate Issued	2005-10-18	view
X0300742	盐酸雷诺嗪片	Ranolazine hydrochloride	Tablet	Chemical Drugs(1.1)	New Drug Application	2003-02-19	哈药集团制药总厂	Harbin Pharmaceutical Group Co Ltd GENERAL Pharm FACTORY	Certificate Issued	2003-10-23	view
CXHL0700059	盐酸雷诺嗪片	Ranolazine hydrochloride	Tablet	Chemical Drugs(1.1)	New Drug Application	2007-04-12	扬子江药业集团有限公司	Yangtze River Pharmaceutical (Group) Co Ltd	Certificate Issued	2008-08-07	view
CXHL0500983	盐酸雷诺嗪	Ranolazine hydrochloride	Active ingredient	Chemical Drugs(1.1)	New Drug Application	2005-06-15	齐鲁制药有限公司	QILU Pharmaceutical Co Ltd	Certificate Issued	2005-10-18	view
CXHL0700058	盐酸雷诺嗪	Ranolazine hydrochloride	Active ingredient	Chemical Drugs(1.1)	New Drug Application	2007-04-12	扬子江药业集团有限公司	Yangtze River Pharmaceutical (Group) Co Ltd	Certificate Issued	2008-08-07	view
X0300741	盐酸雷诺嗪	Ranolazine hydrochloride	Active ingredient	Chemical Drugs(1.1)	New Drug Application	2003-02-19	哈药集团制药总厂	Harbin Pharmaceutical Group Co Ltd GENERAL Pharm FACTORY	Certificate Issued	2003-10-23	view