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
CXHL0502004	盐酸度洛西汀	duloxetine hydrochloride	Active ingredient	Chemical Drugs(3.1)	New Drug Application	2005-12-08	深圳市万欣医药科技开发有限公司	Shenzhen Wanxin Pharmatech Co Ltd	Certificate Issued	2007-01-16	view
CXHL0502005	盐酸度洛西汀肠溶片	duloxetine hydrochloride	Tablet	Chemical Drugs(3.1)	New Drug Application	2005-12-12	深圳市万欣医药科技开发有限公司	Shenzhen Wanxin Pharmatech Co Ltd	Certificate Issued	2007-01-16	view
CXHL0502006	盐酸度洛西汀肠溶微丸胶囊	duloxetine hydrochloride	Capsule	Chemical Drugs(3.1)	New Drug Application	2005-12-12	深圳市万欣医药科技开发有限公司	Shenzhen Wanxin Pharmatech Co Ltd	Certificate Issued	2007-01-16	view
CXHL0600989	异丙肌苷	isoprinosine	Active ingredient	Chemical Drugs(3.1)	New Drug Application	2006-09-14	深圳市万欣医药科技开发有限公司	Shenzhen Wanxin Pharmatech Co Ltd	Certificate Issued	2007-07-11	view
CXHL0600991	异丙肌苷胶囊	isoprinosine	Capsule	Chemical Drugs(3.1)	New Drug Application	2006-09-14	深圳市万欣医药科技开发有限公司	Shenzhen Wanxin Pharmatech Co Ltd	Certificate Issued	2007-07-25	view
CXHL0600990	异丙肌苷片	isoprinosine	Tablet	Chemical Drugs(3.1)	New Drug Application	2006-09-14	深圳市万欣医药科技开发有限公司	Shenzhen Wanxin Pharmatech Co Ltd	Certificate Issued	2007-07-11	view