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
CXS00501	复方丙戊酸钠缓释片	sodium valproate;valproic acid	Tablet, extended release	Chemical Drugs(3)	New Drug Application	2000-10-18	杭州赛诺菲圣德拉堡民生制药有限公司	Sanofi (Hangzhou) Pharmaceutical Co Ltd	Certificate Issued	2001-10-17	view
X0302354	复方丙戊酸钠缓释片	sodium valproate;valproic acid	Tablet, extended release	Chemical Drugs	Supplementary Application	2003-05-04	杭州赛诺菲圣德拉堡民生制药有限公司	Sanofi (Hangzhou) Pharmaceutical Co Ltd	Certificate Issued	2003-09-29	view
X0302335	复方丙戊酸钠缓释片	sodium valproate;valproic acid	Tablet, extended release	Chemical Drugs	Supplementary Application	2004-03-12	杭州赛诺菲圣德拉堡民生制药有限公司	Sanofi (Hangzhou) Pharmaceutical Co Ltd	Certificate Issued	2004-05-28	view
CXHB0690002	复方丙戊酸钠缓释片	sodium valproate;valproic acid	Tablet, extended release	Chemical Drugs	Supplementary Application	2006-02-28	杭州赛诺菲圣德拉堡民生制药有限公司	Sanofi (Hangzhou) Pharmaceutical Co Ltd	In Review	2003-04-29	view