Drug Registration and Acceptance

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Active Ingredient

Acceptance No.

Manufacturers

Acceptance Date

Status Date

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Drug Type

Submission

Evaluation Conclusion

ATC Category

Special Approval Varieties

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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
CXHL1200289	盐酸氨基葡萄糖硫酸软骨素钠片	chondroitin sulfate sodium;glucosamine hydrochloride	Tablet	Chemical Drugs(3.2)	New Drug Application	2012-11-15	北京双鹭药业股份有限公司	Beijing SL Pharmaceutical Co Ltd	Certificate Issued	2015-11-19	view
CXHR1600005	盐酸氨基葡萄糖硫酸软骨素钠片	chondroitin sulfate sodium;glucosamine hydrochloride	Tablet	Chemical Drugs	State Standards	2016-02-01	北京双鹭药业股份有限公司	Beijing SL Pharmaceutical Co Ltd	Certificate Issued	2016-12-08	view
CYHT1400113	硫酸软骨素钠片	chondroitin sulfate sodium	Tablet	Chemical Drugs	Supplementary Application	2019-03-06	浙江诚意药业股份有限公司	Zhejiang Cheng Yi Pharmaceutical Co Ltd	Certificate Issued	2019-03-26	view
CYHT1600009	硫酸软骨素钠片	chondroitin sulfate sodium	Tablet	Chemical Drugs	Supplementary Application	2019-04-17	悦康药业集团有限公司	Youcare Pharmaceutical Group Co Ltd	Certificate Issued	2019-05-15	view