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Metformin – Extended-Release Products - NC Standard
Commercial Utilization Management Policy
Version Date: June 2023

Restricted Product(s)

Restriction applies to brand and generic products

  • Fortamet® (metformin ER osmotic release) 
  • Glumetza® (metformin ER modified release)

FDA Approved Use

  • For adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Criteria for Approval of Restricted Product(s)

  1. The patient has a diagnosis of type 2 diabetes mellitus; AND 
  2. The patient is requesting metformin ER osmotic release (Fortamet)/ brand Fortamet; AND 
    1. The patient has tried and failed or has a clinical contraindication/intolerance to metformin ER (Glucophage XR); OR 
  3. The patient is requesting metformin ER modified release (Glumetza)/brand Glumetza; AND 
    1. The patient has tried and failed or has a clinical contraindication/intolerance to metformin ER (Glucophage XR); AND 
    2. The patient has tried and failed or has a clinical contraindication/intolerance to metformin ER osmotic release (Fortamet); AND 
  4. For formularies that exclude (non-formulary) the requested medication, Non-formulary Exception Criteria applies.

Duration of Approval: 365 days (1 year) 

References

All information referenced is from FDA package insert unless otherwise noted below.

Policy Implementation/Update Information

Criteria and treatment protocols are reviewed annually by the Blue Cross NC P&T Committee, regardless of change. This policy is reviewed in Q2 annually.

June 2023: Criteria update: Formatting changes only.

Feb 2022: Criteria update: Annual criteria review. Updated duration of approval to 1 year.

Nov 2020: Criteria update: Annual criteria review. Formatting changes only.

Mar 2019: Added Net Results to policy – combined all formularies into one policy. Updated duration of approval to 3 years.

Jan 2018: Restriction on brand and generic Fortamet extended to the Enhanced formulary

Oct 2017: Restrictions added to brand and generic Fortamet on the Essential formulary

May 2016: Original utilization management criteria issued

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