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
CXHS1300017	盐酸替利定片	tilidine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2013-02-04	河北奥星集团药业有限公司	HeBei Aoxing Group Pharmaceutical Co Ltd	Certificate Issued	2015-05-27	view
CXHL0600337	盐酸替利定片	tilidine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2006-05-24	河北奥星集团药业有限公司	HeBei Aoxing Group Pharmaceutical Co Ltd	Certificate Issued	2007-04-13	view
CXHS1300018	盐酸替利定片	tilidine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2013-02-04	河北奥星集团药业有限公司	HeBei Aoxing Group Pharmaceutical Co Ltd	Certificate Issued	2015-05-27	view
CXHB0701378	复方盐酸替利定片	naloxone hydrochloride;TILIDINE HYDROCHLORIDE	Tablet	Chemical Drugs	Supplementary Application	2007-10-18	河北奥星集团药业有限公司	HeBei Aoxing Group Pharmaceutical Co Ltd	Certificate Issued	2008-10-21	view
CXHL0600864	复方盐酸替利定片	naloxone hydrochloride;TILIDINE HYDROCHLORIDE	Tablet	Chemical Drugs(3.2)	New Drug Application	2006-09-13	河北奥星集团药业有限公司	HeBei Aoxing Group Pharmaceutical Co Ltd	Certificate Issued	2007-08-29	view