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

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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
CXHB0601646	愈酚伪麻口服溶液	guaifenesin;pseudoephedrine hydrochloride	Oral solution	Chemical Drugs	Supplementary Application	2007-06-07	上海强生制药有限公司	Shanghai Johnson & Johnson Pharmaceuticals Ltd	Certificate Issued	2008-08-14	view
CYHB1102560	愈酚伪麻口服溶液	guaifenesin;pseudoephedrine hydrochloride	Oral solution	Chemical Drugs	Supplementary Application	2011-09-14	上海强生制药有限公司	Shanghai Johnson & Johnson Pharmaceuticals Ltd	Certificate Issued	2012-12-06	view
CYHB1804576	愈酚伪麻口服溶液	guaifenesin;pseudoephedrine hydrochloride	Oral solution	Chemical Drugs	Supplementary Application	2018-09-03	上海强生制药有限公司	Shanghai Johnson & Johnson Pharmaceuticals Ltd	Certificate Issued	2018-11-23	view
CYHB1806915	愈酚伪麻口服溶液	guaifenesin;pseudoephedrine hydrochloride	Oral solution	Chemical Drugs	Supplementary Application	2018-12-29	上海强生制药有限公司	Shanghai Johnson & Johnson Pharmaceuticals Ltd	Certificate Issued	2019-11-19	view