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
CYHB2401915	氨酚氯雷伪麻缓释片	loratadine;paracetamol;Pseudoephedrine Sulfate	Tablet, extended release	Chemical Drugs	Supplementary Application	2024-11-16		Guangzhou Baiyunshan Pharmaceutical Co Ltd Guangzhou Baiyunshan Pharmaceutical General			view
CXHS0900301	氨酚氯雷伪麻缓释片	loratadine;paracetamol;Pseudoephedrine Sulfate	Tablet, extended release	Chemical Drugs(3.2)	New Drug Application	2010-01-18	西安葛蓝新通制药有限公司	Xi'an Gelan Xintong Pharmaceutical Co Ltd;Xi’an Xintong Pharmaceutical Research Co Ltd	Certificate Issued	2011-01-07	view
CXHB0800109	氨酚氯雷伪麻缓释片	loratadine;paracetamol;Pseudoephedrine Sulfate	Tablet, extended release	Chemical Drugs	Supplementary Application	2008-08-18	武汉维奥制药有限公司	Wuhan Wei'ao Pharmaceutical Co Ltd	Certificate Issued	2009-05-05	view
X0407353	氨酚氯雷伪麻缓释片	loratadine;paracetamol;Pseudoephedrine Sulfate	Tablet, extended release	Chemical Drugs(3.2)	New Drug Application	2004-12-03	深圳海王药业有限公司	Shenzhen Neptunus Pharmaceutical Co Ltd;Nanjing Yiren Technology Co Ltd	Certificate Issued	2005-11-25	view