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
CXHL0501486	氨氯地平贝那普利片（Ⅰ）	amlodipine;Benazepril hydrochloride	Tablet	Chemical Drugs(3.2)	New Drug Application	2005-08-11	苏州东瑞制药有限公司	Suzhou Dawnrays Pharmaceutical Co Ltd	Certificate Issued	2006-12-12	view
CXHB1700116	氨氯地平贝那普利片（Ⅰ）	amlodipine;Benazepril hydrochloride	Tablet	Chemical Drugs	Supplementary Application	2018-09-30	扬子江药业集团广州海瑞药业有限公司	YANGTZE River Pharmaceutical Group Guangzhou Hairui Pharmaceutical Co Ltd	Certificate Issued	2020-03-13	view
CXHS1200023	氨氯地平贝那普利片(I)	amlodipine;Benazepril hydrochloride	Tablet	Chemical Drugs(3.2)	New Drug Application	2012-03-29	苏州东瑞制药有限公司	Suzhou Dawnrays Pharmaceutical Co Ltd	Certificate Issued	2015-10-29	view