Viibryd (vilazodone)
Indications for Prior Authorization
Viibryd (vilazodone)
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For diagnosis of Major Depressive Disorder
Indicated for the treatment of major depressive disorder (MDD) in adults.
Criteria
Brand Viibryd
For reauthorization request, bypass criteria review and approve through 12/31/2039 For state-mandated plans in Illinois or other states where applicable: Step therapy requirements do NOT apply. Beginning January 1, 2026, step therapy requirements or use of the authorization of alternative covered medications in a manner that effectively creates a step therapy requirement will not be imposed.
Step Therapy
Length of Approval: When approved; no reauthorization required
- Requested drug is being used for a Food and Drug Administration (FDA)-approved indication AND
- Trial and failure (of a minimum 30-day supply), or intolerance to generic vilazodone
P & T Revisions
1970-01-01, 2025-12-18, 2025-07-02, 2025-05-29, 2024-06-13, 2023-06-19, 2022-10-31
References
- Viibryd prescribing information. Allergan USA, Inc. Madison, NJ. October 2023.
Revision History
- 1970-01-01: No criteria changes
- 2025-12-18: no criteria changes, added IL statute operational note
- 2025-07-02: 2025 Annual Review. No criteria changes. Updated references.
- 2025-05-29: Removing reauthorization requirement as part of extended reauthorization program.
- 2024-06-13: 2024 Annual Review
- 2023-06-19: 2023 Annual Review
- 2022-10-31: New UM Criteria
HEALTHY LIVING