Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: BUPROPION HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB3
Application Number: A211200
Product Number: 002
Approval Date: Apr 29, 2020
Applicant Holder Full Name: ZHEJIANG JUTAI PHARMACEUTICAL CO LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
