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
CXHL0500100	盐酸度洛西汀片	duloxetine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2005-02-17	南京华威医药科技开发有限公司	Nanjing Huawei Medicine Technology Development Co Ltd	Certificate Issued	2005-09-16	view
CXHL0501144	盐酸度洛西汀片	duloxetine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2005-06-10	长春高新百克药物研究院有限公司	Cchn Bcht Pharmaceutical Research Institute Co Ltd	Certificate Issued	2006-04-10	view
CXHL0501285	盐酸度洛西汀片	duloxetine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2005-08-04	扬子江药业集团有限公司	Yangtze River Pharmaceutical (Group) Co Ltd	Certificate Issued	2006-06-28	view
CXHL0501424	盐酸度洛西汀片	duloxetine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2005-08-09	北京德众万全医药科技有限公司	Beijing Dezhong Wanquan Medicine Technology Co Ltd	Certificate Issued	2006-06-28	view
CXHL0502237	盐酸度洛西汀片	duloxetine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2006-02-07	海南盛科生命科学研究院	Hainan Sinican Life Science Institute	Certificate Issued	2006-12-12	view