Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: ZYBAN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020711
Product Number: 003
Approval Date: May 14, 1997
Applicant Holder Full Name: GLAXOSMITHKLINE
Marketing Status:
Discontinued
Patent and Exclusivity Information