Active Ingredient: DESVENLAFAXINE SUCCINATE
Proprietary Name: DESVENLAFAXINE SUCCINATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 100MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A204083
Product Number: 001
Approval Date: Feb 16, 2016
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
