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
CYHS1100555	盐酸马普替林片	maprotiline hydrochloride	Tablet	Chemical Drugs(6)	Generic Drug	2011-09-27	陕西步长制药有限公司	Shaanxi Buchang Pharmaceutical Co Ltd	Certificate Issued	2015-11-05	view
JYHZ0800007	盐酸马普替林	maprotiline hydrochloride	Active ingredient	Chemical Drugs	License Renew	2008-01-15	Novartis Pharma AG	Novartis Pharma Schweiz AG	Certificate Issued	2008-08-06	view
J0400818	盐酸马普替林	maprotiline hydrochloride	Active ingredient	Chemical Drugs	Supplementary Application	2004-12-23		Beijing Novartis Pharma Co Ltd	Certificate Issued	2005-04-29	view
Y0405082	盐酸马普替林	maprotiline hydrochloride	Active ingredient	Chemical Drugs(6)	Generic Drug	2004-07-20	山东潍坊制药厂有限公司	ZHONGFU Pharmaceutical Co Ltd	Certificate Issued	2005-04-29	view
J0300205	盐酸马普替林	maprotiline hydrochloride	Active ingredient	Chemical Drugs	License Renew	2003-03-11	香港诺华制药有限公司北京代表处		Approval Completed-Pending Certificated	2003-10-08	view