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: AB2
Application Number: A075914
Product Number: 001
Approval Date: May 27, 2004
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information
