Active Ingredient: TRAZODONE HYDROCHLORIDE
Proprietary Name: TRAZODONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A072192
Product Number: 001
Approval Date: Feb 2, 1989
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
