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: Yes
TE Code: AB2
Application Number: A079094
Product Number: 001
Approval Date: Mar 24, 2009
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status:
Prescription
Patent and Exclusivity Information