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
CXL01500	盐酸氟西汀片	fluoxetine hydrochloride	Tablet	Chemical Drugs(5)	New Drug Application	2001-06-15	常州四药制药有限公司	Changzhou Siyao Pharmaceuticals Co Ltd	Certificate Issued	2001-12-20	view
CYHB0601964	盐酸氟西汀片	fluoxetine hydrochloride	Tablet	Chemical Drugs	Supplementary Application	2007-03-19	常州四药制药有限公司	Changzhou Siyao Pharmaceuticals Co Ltd	Certificate Issued	2008-01-03	view
CXHL1501092	奥氮平盐酸氟西汀片	fluoxetine hydrochloride;olanzapine	Tablet	Chemical Drugs(3.2)	New Drug Application	2015-07-31	沈阳华泰药物研究有限公司	Shenyang Huatai Medication Research Co Ltd	Certificate Issued	2016-08-12	view
CXHL1501093	奥氮平盐酸氟西汀片	fluoxetine hydrochloride;olanzapine	Tablet	Chemical Drugs(3.2)	New Drug Application	2015-07-31	沈阳华泰药物研究有限公司	Shenyang Huatai Medication Research Co Ltd	Certificate Issued	2016-08-12	view