Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: BUPROPION HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A076143
Product Number: 002
Approval Date: Jan 17, 2006
Applicant Holder Full Name: APOTEX INC ETOBICOKE SITE
Marketing Status:
Prescription
Patent and Exclusivity Information