Tyrvaya (varenicline solution)

Indications for Prior Authorization

Tyrvaya (varenicline solution) nasal spray
  • For diagnosis of Dry Eye Disease
    Indicated for the treatment of the signs and symptoms of dry eye disease.

Criteria

Tyrvaya

For initial authorization request, approve through 12/31/2039 For reauthorization request, bypass criteria review and approve through 12/31/2039

Prior Authorization

Length of Approval: When approved; no reauthorization required

  • Diagnosis of dry eye disease
  • AND
  • Trial and failure, contraindication, or intolerance to one of the following:
    • Brand Restasis (cyclosporine 0.05%)
    • Xiidra (lifitegrast)
P & T Revisions

1970-01-01, 2025-05-27, 2024-09-04, 2024-05-29, 2023-10-26, 2023-09-10, 2022-06-01, 2021-11-17

  1. Tyrvaya Prescribing Information. Oyster Point Pharma, Inc. Princeton, NJ. October 2021.
  2. American Academy of Ophthalmology. Dry Eye Syndrome Preferred Practice Pattern. October 2018. Available at https://www.aaojournal.org/article/S0161-6420(18)32650-2/fulltext#tbl3. Accessed November 4, 2021.
  3. Wood, S., Mian, S. Diagnostic Tools for Dry Eye Disease. Available at https://www.touchophthalmology.com/wp-content/uploads/sites/16/2017/01/Diagnostic-Tools-for-Dry-Eye-Disease_1.pdf. Accessed Nov 9. 2021.
  4. Zeev, M., Miller, D, et al. Diagnosis of dry eye disease and emerging technologies. Clin Ophthalmol 2014;8:581-590. Available at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964175/#b16-opth-8-581. Accessed November 9, 2021.

  • 2025-05-27: Removing reauthorization requirement as part of extended reauthorization program.
  • 2024-09-04: update guideline
  • 2024-05-29: update guideline
  • 2023-10-26: Program update to standard reauthorization language. No changes to clinical intent.
  • 2023-09-10: 2023 Annual Review.
  • 2022-06-01: Removed requirement for paid claims/submission of medical records.
  • 2021-11-17: 2022 New PA UM Criteria

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