Approved Hospital Formulary
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Approved Hospital Formulary
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buprenorphine

buprenorphine
Drug Name Form Strength Notes
Butrans Transdermal System (non-formulary) FILM, EXTENDED RELEASE, TRANSDERMAL 10 mcg/hr
Buprenex SOLUTION, INJECTABLE 0.3 mg/mL
Buprenorphine SOLUTION, INJECTABLE 0.3 mg/mL
Buprenorphine TABLET, SUBLINGUAL 2 mg
Buprenorphine TABLET, SUBLINGUAL 8 mg
Belbuca FILM, BUCCAL Belbuca (buccal film of choice for formulary)
Brixadi Monthly SOLUTION, EXTENDED RELEASE, SUBCUTANEOUS -
Brixadi Weekly SOLUTION, EXTENDED RELEASE, SUBCUTANEOUS -
Sublocade SOLUTION, EXTENDED RELEASE, SUBCUTANEOUS -


Additional Information:

Management of Opioid Use Disorder: See Practice Guideline 900.5034

Buprenorphine Patch (Butrans) is Formulary Restricted to continuation of PTA therapy

 

Subcutaneous buprenorphine extended‐release:

    • SUBLOCADE® is Restricted as below:
      • Ambulatory:  For clinics (typically primary care, Pain Clinics and Project Nurture); due to REMS program, only to be filled through Legacy Apothecary. 
      • Inpatient: Non-formulary
      • See Legacy Health REMS Requirements for detail.
    • BRIXADI® is Formulary Restricted as below:
      • Weekly Formulation is limited to outpatient clinics, PES (Psychiatric Emergency Services), and ESUDS (Emergency Substance Use Disorder Service), and LEMC Inpatient Pilot Program.
      • Monthly formulation will be limited to outpatient clinics and LEMC Inpatient Pilot Program
      • Planned transition to sublingual buprenorphine during inpatient stays.
      • The goal of the Brixadi REMS is to mitigate the risk of serious harm or death that could result from intravenous self-administration, and includes health care setting, pharmacy and wholesaler-distributor requirements for dispensing.
      • See Legacy Health REMS Requirements for detail.

 

 

Drug Name Common Side Effects

Buprenorphine

  • sedation
  • dizziness, headache
  • nausea, vomiting

 


Last updated: Apr. 29, 2026


Class III






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