Active Ingredient: VENLAFAXINE HYDROCHLORIDE
Proprietary Name: VENLAFAXINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A213927
Product Number: 001
Approval Date: Jan 21, 2021
Applicant Holder Full Name: DEXCEL PHARMA TECHNOLOGIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information