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HCSC · Type 2 Diabetes

HCSC coverage for Ozempic (Type 2 Diabetes)

Employer / Commercial Insurance

Covered (preferred drug)

What you need to qualify

  • A1C of 6.5% or higher
  • Lab results confirming eligibility

Qualification pathways

You can qualify through any one of these.

Initial Approval – Preferred Agent (Ozempic/semaglutide is preferred)

All of:

  • Diagnosis of type 2 diabetes
  • Diagnosis confirmed by lab: A1C >= 6.5%, OR fasting plasma glucose >= 126 mg/dL, OR 2-hour plasma glucose >= 200 mg/dL during OGTT, OR random plasma glucose >= 200 mg/dL with symptoms of hyperglycemia
  • Patient will NOT use requested agent in combination with a DPP-4 containing agent
  • Patient will NOT use requested agent in combination with another GLP-1 receptor agonist
  • Patient does NOT have any FDA labeled contraindications to the requested agent
  • Patient age is within FDA labeling for the requested indication OR there is support for use at patient's age

Plus any one of:

  • Request is for a BCBS IL Fully Insured, ASO Cost/BBF, HIM, or Non-ERISA ASO/Self-insured Municipalities/Counties member
  • Prescriber states patient is currently stable on the requested agent
  • Requested agent is a preferred GLP-1 or GLP-1/GIP receptor agonist

Alternative Approval – BCBS NM Fully Insured or NM HIM Rare Disease

All of:

  • Request is for a BCBS NM Fully Insured or NM HIM member
  • Patient does NOT have any FDA labeled contraindications to the requested agent
  • Requested indication is a rare disease

Plus any one of:

  • Patient has another FDA labeled indication for the requested agent and route of administration
  • Patient has another indication supported in compendia for the requested agent and route of administration

Alternative Approval – Ohio Fully Insured or HIM Shop (SG)

All of:

  • Member resides in Ohio
  • Plan is Fully Insured or HIM Shop (SG)
  • Patient does NOT have any FDA labeled contraindications to the requested agent

Plus any one of:

  • Patient has another FDA labeled indication for the requested agent and route of administration
  • Patient has another indication supported in compendia for the requested agent and route of administration
  • Prescriber has submitted TWO articles from major peer-reviewed professional medical journals supporting the proposed use as generally safe and effective

Documentation to bring

  • Chart notes or copy of lab test results confirming T2DM diagnosis (A1C >= 6.5%, fasting plasma glucose >= 126 mg/dL, 2-hour plasma glucose >= 200 mg/dL during OGTT, or random plasma glucose >= 200 mg/dL with symptoms)
  • Documentation that patient will not use requested agent with a DPP-4 containing agent
  • Documentation that patient will not use requested agent with another GLP-1 receptor agonist
  • Documentation of absence of FDA labeled contraindications

Quantity limits

  • 2 MG/3ML — 1 pen per 28 days
  • 4 MG/3ML — 1 pen per 28 days
  • 8 MG/3ML — 1 pen per 28 days

Approval and renewal

  • Initial approval: 12 months
  • Renewal: every 12 months
  • To renew, the plan looks for Patient must have demonstrated clinical benefit with a targeted GLP-1 agent. Prior A1C/lab confirmation and step therapy requirements are NOT re-verified at renewal; only clinical benefit, preferred/non-preferred step therapy status, no DPP-4 combination, no dual GLP-1, and no contraindications are checked.

Not covered when

  • Concurrent use with DPP-4 containing agents (e.g., Januvia, Onglyza, Tradjenta, Nesina, and combination products)
  • Concurrent use with another GLP-1 receptor agonist (e.g., Saxenda, Wegovy, Zepbound, Mounjaro, etc.)
  • FDA labeled contraindications to the requested agent

Exceptions

  • Ohio: Ohio Fully Insured or HIM Shop (SG) members may qualify under Ohio alternative pathway
  • BCBSIL: Approval duration 12 months; BCBS IL Fully Insured, ASO Cost/BBF, HIM, or Non-ERISA ASO/Self-insured Municipalities/Counties members may qualify without standard step therapy
  • BCBSOK: Approval duration 36 months (initial and renewal)
  • BCBS_NM: NM Fully Insured or NM HIM members may qualify under rare disease alternative pathway

Policy note: Ozempic (semaglutide injectable) is listed as a PREFERRED agent. Rybelsus (oral semaglutide) shares the same clinical criteria and is also covered under this policy. Quantity limit: fill limit of one injectable GLP-1 agent and one strength per 28 days; refill window applies. Oral semaglutide (Rybelsus) subject to fill limit of one oral GLP-1 agent and one strength per 28 days. When a non-preferred agent requests approval, Ozempic/Rybelsus serves as one of the preferred step therapy agents that must have been tried. BCBSOK approval is 36 months.

Policy effective May 11, 2026 · verified June 2, 2026 · source: HCSC_GLP-1_Agonists_ProgSum.pdf

ACA Marketplace

Covered (preferred drug)

What you need to qualify

  • A1C of 6.5% or higher
  • Lab results confirming eligibility

Qualification pathways

You can qualify through any one of these.

Initial Approval – Preferred Agent (Ozempic/semaglutide is preferred)

All of:

  • Diagnosis of type 2 diabetes
  • Diagnosis confirmed by lab: A1C >= 6.5%, OR fasting plasma glucose >= 126 mg/dL, OR 2-hour plasma glucose >= 200 mg/dL during OGTT, OR random plasma glucose >= 200 mg/dL with symptoms of hyperglycemia
  • Patient will NOT use requested agent in combination with a DPP-4 containing agent
  • Patient will NOT use requested agent in combination with another GLP-1 receptor agonist
  • Patient does NOT have any FDA labeled contraindications to the requested agent
  • Patient age is within FDA labeling for the requested indication OR there is support for use at patient's age

Plus any one of:

  • Request is for a BCBS IL Fully Insured, ASO Cost/BBF, HIM, or Non-ERISA ASO/Self-insured Municipalities/Counties member
  • Prescriber states patient is currently stable on the requested agent
  • Requested agent is a preferred GLP-1 or GLP-1/GIP receptor agonist

Alternative Approval – BCBS NM Fully Insured or NM HIM Rare Disease

All of:

  • Request is for a BCBS NM Fully Insured or NM HIM member
  • Patient does NOT have any FDA labeled contraindications to the requested agent
  • Requested indication is a rare disease

Plus any one of:

  • Patient has another FDA labeled indication for the requested agent and route of administration
  • Patient has another indication supported in compendia for the requested agent and route of administration

Alternative Approval – Ohio Fully Insured or HIM Shop (SG)

All of:

  • Member resides in Ohio
  • Plan is Fully Insured or HIM Shop (SG)
  • Patient does NOT have any FDA labeled contraindications to the requested agent

Plus any one of:

  • Patient has another FDA labeled indication for the requested agent and route of administration
  • Patient has another indication supported in compendia for the requested agent and route of administration
  • Prescriber has submitted TWO articles from major peer-reviewed professional medical journals supporting the proposed use as generally safe and effective

Documentation to bring

  • Chart notes or copy of lab test results confirming T2DM diagnosis (A1C >= 6.5%, fasting plasma glucose >= 126 mg/dL, 2-hour plasma glucose >= 200 mg/dL during OGTT, or random plasma glucose >= 200 mg/dL with symptoms)
  • Documentation that patient will not use requested agent with a DPP-4 containing agent
  • Documentation that patient will not use requested agent with another GLP-1 receptor agonist
  • Documentation of absence of FDA labeled contraindications

Quantity limits

  • 2 MG/3ML — 1 pen per 28 days
  • 4 MG/3ML — 1 pen per 28 days
  • 8 MG/3ML — 1 pen per 28 days

Approval and renewal

  • Initial approval: 12 months
  • Renewal: every 12 months
  • To renew, the plan looks for Patient must have demonstrated clinical benefit with a targeted GLP-1 agent. Prior A1C/lab confirmation and step therapy requirements are NOT re-verified at renewal; only clinical benefit, preferred/non-preferred step therapy status, no DPP-4 combination, no dual GLP-1, and no contraindications are checked.

Not covered when

  • Concurrent use with DPP-4 containing agents (e.g., Januvia, Onglyza, Tradjenta, Nesina, and combination products)
  • Concurrent use with another GLP-1 receptor agonist (e.g., Saxenda, Wegovy, Zepbound, Mounjaro, etc.)
  • FDA labeled contraindications to the requested agent

Exceptions

  • Ohio: Ohio Fully Insured or HIM Shop (SG) members may qualify under Ohio alternative pathway
  • BCBSIL: Approval duration 12 months; BCBS IL Fully Insured, ASO Cost/BBF, HIM, or Non-ERISA ASO/Self-insured Municipalities/Counties members may qualify without standard step therapy
  • BCBSOK: Approval duration 36 months (initial and renewal)
  • BCBS_NM: NM Fully Insured or NM HIM members may qualify under rare disease alternative pathway

Policy note: Ozempic (semaglutide injectable) is listed as a PREFERRED agent. Rybelsus (oral semaglutide) shares the same clinical criteria and is also covered under this policy. Quantity limit: fill limit of one injectable GLP-1 agent and one strength per 28 days; refill window applies. Oral semaglutide (Rybelsus) subject to fill limit of one oral GLP-1 agent and one strength per 28 days. When a non-preferred agent requests approval, Ozempic/Rybelsus serves as one of the preferred step therapy agents that must have been tried. BCBSOK approval is 36 months.

Policy effective May 11, 2026 · verified June 2, 2026 · source: HCSC_GLP-1_Agonists_ProgSum.pdf

All Ozempic policies under HCSC · Check your card