High-Cost Brand with Generics Program

Indications for Prior Authorization

Criteria

Drugs included on the High Cost Brand with Generics List for which a Drug-Specific Prior Authorization Guideline is Unavailable*

Prior Authorization

Length of Approval: 6 Month(s)

  • One of the following:
    • All of the following:
      • Requested drug is FDA-approved for the condition being treated
      • AND
      • Additional requirements listed in the "Indications and Usage" sections of the prescribing information (or package insert) have been met (e.g., first line therapies have been tried and failed, any testing requirements have been met, etc.)
      • AND
      • Requested drug will be used at a dose which is within FDA recommendations
      OR
    • If requested for an off-label indication, the off-label guideline approval criteria have been met
    AND
  • All of the following:
    • Patient has experienced intolerance (e.g., allergy to excipient) with the generic of the requested Brand
    • AND
    • If the requested drug is a Brand fixed-dose combination product, patient has experienced intolerance (e.g., allergy to excipient) with the individual generics in the combination product separately
    • AND
    • Submission of records (e.g., chart notes) confirming why the Brand is expected to provide benefit when the generic product has not been shown to be effective despite having the same active ingredient
    AND
  • One of the following:**
    • Patient has tried and failed at least 4 additional lower tier alternatives within the same therapeutic class. If less than 4 lower tier alternative within the therapeutic class is available, the patient must have tried all lower tier alternatives within the therapeutic class AND additional lower tier alternatives to a total of four. If there are no lower tier alternatives within the same therapeutic class, the patient must have failed 4 lower tier alternatives or have a contraindication or intolerance to all lower tier alternatives
    • OR
    • No lower tier alternative is available to treat the patient's condition
P & T Revisions

2026-09-21, 2024-06-20


  • 2026-09-21: Criteria update to require up to 5 formulary alternatives where available
  • 2024-06-20: New Program