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:
Application Number: A214423
Product Number: 001
Approval Date: Jan 4, 2022
Applicant Holder Full Name: SUNNY PHARMTECH INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
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:
Application Number: A214423
Product Number: 002
Approval Date: Jan 4, 2022
Applicant Holder Full Name: SUNNY PHARMTECH INC
Marketing Status:
Discontinued
Patent and Exclusivity Information