CFDA Approvals(Domestic) - DRUGDATAEXPY

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Drug Name	Active Ingredient	Dosage Form	Strength	Manufacturers	Manufacturers	Approval No.	Same Variety(Same Strength)	Approval Date	Drug Classification	Details
盐酸度洛西汀肠溶片	duloxetine hydrochloride	Tablet	20mg(按度洛西汀计)	江苏恩华药业股份有限公司	Jiangsu Nhwa Pharmaceutical Co Ltd	国药准字H20130056	view	2018-06-20	Medicare(class B)	view
盐酸度洛西汀肠溶片	duloxetine hydrochloride	Tablet	20mg(按C18H19NOS计)	上海上药中西制药有限公司	SPH Zhongxi Pharmaceutical Co Ltd	国药准字H20061261	view	2021-07-05	Medicare(class B)	view