Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: BUPROPION HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A203013
Product Number: 002
Approval Date: Jun 8, 2018
Applicant Holder Full Name: ALEMBIC PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information