Zurzuvae (zuranolone)

Indications for Prior Authorization

Zurzuvae (zuranolone)
  • For diagnosis of Postpartum Depression (PPD)
    Indicated for the treatment of PPD in women 18 years of age and older

Criteria

Zurzuvae

Prior Authorization

Length of Approval: 14 Day(s)

  • One of the following:
    • Diagnosis of moderate to severe postpartum depression (PPD)
    • OR
    • Both of the following:
      • Diagnosis of mild postpartum depression (PPD)
      • AND
      • Trial and failure, contraindication or intolerance to at least one oral SSRI or SNRI (e.g., escitalopram, duloxetine)
    AND
  • Patient is 18 years of age or older
  • AND
  • Onset of symptoms in the third trimester or within 4 weeks of delivery
  • AND
  • Prescriber attests that the patient has been counseled and has agreed to adhere to the following: Will follow instructions to not drive or operate machinery until at least 12 hours after taking each dose of Zurzuvae for the duration of the 14-day treatment course and that patients are informed that they may not be able to assess their own driving competence or the degree of driving impairment caused by Zurzuvae
P & T Revisions

2025-01-20, 2024-09-19, 2024-01-04

  1. Zurzuvae Prescribing Information. Biogen MA Inc. July 2024.

  • 2025-01-20: 2025 annual review. No clinical changes.
  • 2024-09-19: Removal of trial requirement for moderate PPD to support formulary strategy.
  • 2024-01-04: New Program