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
CXS20020179	复方氯雷他定缓释片	loratadine;Pseudoephedrine Sulfate	Tablet, extended release	Chemical Drugs(4)	New Drug Application	2003-08-27	南京臣功制药有限公司桂林集琦药业股份有限公司	Sealand Securities Co Ltd	Certificate Issued	2004-04-02	view
CXL01G97	复方氯雷他定缓释片	loratadine;Pseudoephedrine Sulfate	Tablet, extended release	Chemical Drugs(4)	New Drug Application	2001-12-14	北京德众万全药物技术开发有限公司	Beijing Dezhong Wanquan Pharmaceutical Technology Development Co Ltd	Certificate Issued	2003-07-07	view
CXL01515	复方氯雷他定缓释片(12hr)	loratadine;Pseudoephedrine Sulfate	Tablet, extended release	Chemical Drugs(2)	New Drug Application	2001-06-27	山东诚创医药技术开发有限公司	Shandong Chengchuang Pharmaceutical Technology Development Co Ltd	Approval Completed-Pending Certificated	2002-11-29	view