Non-Solid Oral Dosage Forms
Indications for Prior Authorization
Criteria
Norliqva
Prior Authorization
Length of Approval: 12 Month(s)
- One of the following:
- Requested drug is FDA-approved for the condition being treated OR
- If requested for an off-label indication, the off-label guideline approval criteria have been met
- Patient is unable to swallow a solid dosage form (e.g., oral tablet, capsule) due to one of the following:
- Age
- Physical impairment (e.g., difficulties with motor or oral coordination)
- Dysphagia
- Patient is using a feeding tube or nasal gastric tube
Atorvaliq, Gloperba, Likmez, generic spironolactone suspension
Prior Authorization
Length of Approval: 12 Month(s)
- One of the following:
- Requested drug is FDA-approved for the condition being treated OR
- If requested for an off-label indication, the off-label guideline approval criteria have been met
- One of the following:
- Trial and failure, or intolerance to a generic equivalent of the requested drug in a solid dosage form OR
- Patient is unable to swallow a solid dosage form (e.g., oral tablet, capsule) due to one of the following:
- Age
- Physical impairment (e.g., difficulties with motor or oral coordination)
- Dysphagia
- Patient is using a feeding tube or nasal gastric tube
Jylamvo, Xatmep, Zonisade
Prior Authorization
Length of Approval: 12 Month(s)
- One of the following:
- Requested drug is FDA-approved for the condition being treated OR
- If requested for an off-label indication, the off-label guideline approval criteria have been met
- One of the following:
- Trial and failure, or intolerance to a generic equivalent of the requested drug in a solid dosage form OR
- Patient is unable to swallow a solid dosage form (e.g., oral tablet, capsule) due to one of the following:
- Age
- Physical impairment (e.g., difficulties with motor or oral coordination)
- Dysphagia
- Patient is using a feeding tube or nasal gastric tube
- For continuation of prior therapy
P & T Revisions
2024-09-11, 2024-06-28, 2024-05-06, 2024-01-31, 2024-01-03, 2023-11-29, 2023-08-28, 2023-03-27, 2022-10-24, 2022-10-05
References
Revision History
- 2024-09-11: 2024 UM Annual Review. Addition of COT option for Jylamvo, Xatmep and Zonisade due to COT policy. Removal of PA from Myhibbin
- 2024-06-28: Addition of Myhibbin to guideline
- 2024-05-06: Addition of Xatmep as a target agent
- 2024-01-31: Addition of Gloperba as target
- 2024-01-03: Addition of Jylamvo
- 2023-11-29: Addition of Likmez and generic Carospir (spironolactone suspension)
- 2023-08-28: 2023 UM Annual Review. No changes
- 2023-03-27: update guideline
- 2022-10-24: update guideline
- 2022-10-05: New PA program.