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
CXS01351	盐酸西替利嗪	cetirizine hydrochloride	Active ingredient	Chemical Drugs(4)	New Drug Application	2001-07-27	合肥医药医药研究所苏州中化药品工业有限公司		Certificate Issued	2003-05-30	view
CXS01353	盐酸西替利嗪分散片	cetirizine hydrochloride	Tablet	Chemical Drugs(4)	New Drug Application	2001-07-27	合肥医药医药研究所	Hefei Medical and Pharmaceutical Co Ltd	Approval Completed-Pending Certificated	2003-05-09	view
CXS01352	盐酸西替利嗪片	cetirizine hydrochloride	Tablet	Chemical Drugs(4)	New Drug Application	2001-07-27	合肥医药医药研究所苏州中化药品工业有限公司		Certificate Issued	2003-05-30	view