Active Ingredient: VENLAFAXINE BESYLATE
Proprietary Name: VENLAFAXINE BESYLATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 112.5MG BASE
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N215429
Product Number: 001
Approval Date: Jun 29, 2022
Applicant Holder Full Name: ALMATICA PHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
