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
X0303922	复方盐酸西替利嗪缓释片	cetirizine hydrochloride;pseudoephedrine hydrochloride	Tablet, extended release	Chemical Drugs(3.2)	New Drug Application	2004-04-13	苏州东瑞制药有限公司	Suzhou Dawnrays Pharmaceutical Co Ltd	Certificate Issued	2004-07-09	view
X0301499	复方盐酸西替利嗪缓释片	cetirizine hydrochloride;pseudoephedrine hydrochloride	Tablet, extended release	Chemical Drugs(3.2)	New Drug Application	2003-03-26	北京瑞康医药技术有限公司	Beijing Ruikang Medicine Technology Co Ltd	Certificate Issued	2003-12-05	view