Applies to Employer plans.
Covered (preferred drug)Qualification pathways
You can qualify through any one of these.
New patient - prior therapy requirement
All of:
- Diagnosis of type 2 diabetes mellitus (medical record documentation required)
- Requested product will not be taken concomitantly with a DPP-4 containing agent
- Requested product will not be taken concomitantly with another GLP-1 agonist
Plus any one of:
- Patient has tried and had an inadequate response, intolerance, or hypersensitivity to an agent containing metformin, sulfonylurea, or insulin
- Patient has an FDA labeled contraindication to metformin
- Patient has a diagnosis of, or is at high risk for, atherosclerotic cardiovascular disease, heart failure, chronic kidney disease, and/or MASH
Continuity of care - currently on therapy
All of:
- Diagnosis of type 2 diabetes mellitus (medical record documentation required)
- Prescriber states patient is currently being treated with the requested agent within the past 90 days and is at risk if therapy is changed
- Requested product will not be taken concomitantly with a DPP-4 containing agent
- Requested product will not be taken concomitantly with another GLP-1 agonist
Documentation to bring
- Medical record documentation of type 2 diabetes mellitus diagnosis
- Documentation of prior trial with inadequate response, intolerance, or hypersensitivity to metformin, sulfonylurea, or insulin OR FDA labeled contraindication to metformin OR diagnosis of/high risk for ASCVD, heart failure, CKD, or MASH (OR attestation that patient is currently on this agent within the past 90 days and at risk if changed)
- Attestation that requested product will not be taken concomitantly with a DPP-4 containing agent
- Attestation that requested product will not be taken concomitantly with another GLP-1 agonist
Quantity limits
- 2.5mg/0.5mL — 2 mL (4 pens)
- 5mg/0.5mL — 2 mL (4 pens)
- 7.5mg/0.5mL — 2 mL (4 pens)
- 10mg/0.5mL — 2 mL (4 pens)
- 12.5mg/0.5mL — 2 mL (4 pens)
- 15mg/0.5mL — 2 mL (4 pens)
Approval and renewal
- Initial approval: 12 months
- Renewal: every 12 months
Not covered when
- Concomitant use with DPP-4 containing agent
- Concomitant use with another GLP-1 agonist
Policy note: Mounjaro is listed as a preferred product per the April 2023 policy update. Indication expanded to include pediatric patients 10 years and older per Jan 2026 update. Approved for T2DM only per this policy; weight loss is not an approved indication under this policy document.
Policy effective May 1, 2026 · verified June 2, 2026 · source: GLP-1 Agonists Nc Standard · View policy document (PDF)