Active Ingredient: VENLAFAXINE HYDROCHLORIDE
Proprietary Name: VENLAFAXINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 150MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214609
Product Number: 001
Approval Date: Jun 30, 2021
Applicant Holder Full Name: APPCO PHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: VENLAFAXINE HYDROCHLORIDE
Proprietary Name: VENLAFAXINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 225MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214609
Product Number: 002
Approval Date: Jun 30, 2021
Applicant Holder Full Name: APPCO PHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information