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
J0301591	盐酸帕罗西汀控释片	paroxetine hydrochloride	Tablet, extended release	Chemical Drugs(3.1)	Import Drug Application	2004-05-31		GlaxoSmithKline (China) Investment Co Ltd	Certificate Issued	2004-09-14	view
J0301590	盐酸帕罗西汀控释片	paroxetine hydrochloride	Tablet, extended release	Chemical Drugs(3.1)	Import Drug Application	2004-05-31		GlaxoSmithKline (China) Investment Co Ltd	Certificate Issued	2004-09-14	view
JXHS0800070	盐酸帕罗西汀控释片	paroxetine hydrochloride	Tablet, extended release	Chemical Drugs	Import Drug Application	2008-12-25	GLAXOSMITHKLINE INC.	Glaxosmithkline Inc;Smithkline Beecham (Cork) Ltd	Certificate Issued	2010-08-18	view
JXHS0800071	盐酸帕罗西汀控释片	paroxetine hydrochloride	Tablet, extended release	Chemical Drugs	Import Drug Application	2008-12-25	GLAXOSMITHKLINE INC.	Glaxosmithkline Inc;Smithkline Beecham (Cork) Ltd	Certificate Issued	2010-08-18	view