Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: FORFIVO XL
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 450MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N022497
Product Number: 001
Approval Date: Nov 10, 2011
Applicant Holder Full Name: TWI PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
