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
CYHS1800275	苯丁酸钠片	sodium phenylbutyrate	Tablet	Chemical Drugs(3)	Generic Drug	2018-09-19	兆科药业（广州）有限公司	Zhaoke Pharmaceutical (Guangzhou) Co Ltd	Certificate Issued	2021-10-29	view
CXHL1200045	苯丁酸钠片	sodium phenylbutyrate	Tablet	Chemical Drugs(3.1)	New Drug Application	2012-04-05	北京依诺泰药物化学技术有限公司	Beijing Yinuotai Pharmacy Chemistry Technology Co Ltd	Certificate Issued	2014-07-02	view
CXHL0900401	苯丁酸钠片	sodium phenylbutyrate	Tablet	Chemical Drugs(3.1)	New Drug Application	2009-12-23	北京恒瑞康达医药科技发展有限公司	Beijing Hengrui Kangda Medicine Technology Development Co Ltd	Certificate Issued	2012-03-23	view
CXHL0800059	苯丁酸钠片	sodium phenylbutyrate	Tablet	Chemical Drugs(3.1)	New Drug Application	2008-06-12	浙江贝达药业有限公司	Betta Pharmaceuticals Co Ltd	Certificate Issued	2010-01-27	view
CXHS1500015	苯丁酸钠片	sodium phenylbutyrate	Tablet	Chemical Drugs(3.1)	New Drug Application	2015-05-05	贝达药业股份有限公司	Betta Pharmaceuticals Co Ltd	Certificate Issued	2021-04-20	view