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Buprenorphine

Brand names: Brixadi, Sublocade, Buprenorphine, Butrans

Partial Opioid Agonist Subcutaneous Controlled substance, schedule III

At a glance

Medicare prescriptions, 2024
417,889
Medicare drug cost
$135.7M
Average cost per prescription
$325
Clinicians who prescribed it
9,819

Where it is prescribed

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List the prescribers in any state, county, city or ZIP code →

What it is used for

SUBLOCADE is indicated for the treatment of moderate to severe opioid use disorder in patients who have initiated treatment with a single dose of a transmucosal buprenorphine product or who are already being treated with buprenorphine. SUBLOCADE should be used as part of a complete treatment plan that includes counseling and psychosocial support.

From the FDA-approved prescribing information (label dated July 2026). Full labels on DailyMed (opens in a new tab)

Boxed warning

WARNING: RISK OF SERIOUS HARM OR DEATH WITH INTRAVENOUS ADMINISTRATION; SUBLOCADE RISK EVALUATION AND MITIGATION STRATEGY Serious harm or death could result if administered intravenously. SUBLOCADE forms a solid mass upon contact with body fluids and may cause occlusion, local tissue damage, and thrombo-embolic events, including life threatening pulmonary emboli, if administered intravenously. Because of the risk of serious harm or death that could result from intravenous self-administration, SUBLOCADE is only available through a restricted program called the SUBLOCADE REMS Program. Healthcare settings and pharmacies that order and dispense SUBLOCADE must be certified in this program and comply with the REMS requirements.

The FDA’s strongest warning on a label. It doesn’t mean the drug is unsafe for most people; talk to your doctor or pharmacist before stopping or changing any medicine.

Who prescribes it

All prescribers, by place, name or specialty →

Share of Medicare prescriptions written by each specialty. Select one to list its prescribers.

Trend, 2019–2024

Medicare prescriptions rose 101% from 2019 to 2024.

Medicare Part D prescriptions per year, all prescribers
  • 2019255,389
  • 2020274,551
  • 2021312,840
  • 2022358,811
  • 2023423,135
  • 2024513,391

Biggest change by state since 2019

  • Washington +201%
  • Tennessee +149%
  • Arizona +143%
  • South Carolina +120%
  • Pennsylvania +116%
  • Florida (smallest change) +48%
  • Texas (smallest change) +71%

From CMS’s yearly state and national Part D summaries, which count every prescriber, including those CMS leaves out of its per-clinician data (fewer than 11 prescriptions). That is why these totals are higher than the count at the top of this page. Prescriptions include refills.

What it looks like

Pills from 2 makers on file. The same medicine can look different depending on who made it, so check the imprint (the letters and numbers on the pill) with your pharmacist if a refill looks different.

Golden State Medical Supply, Inc.

StrengthLooks likeImprint
2 mg / 0.5 mg naloxone hydrochloride dihydrateorange round tablet, 6 mm54 122
8 mg / 2 mg naloxone hydrochloride dihydrateorange round tablet, 10 mm54 375

Major Pharmaceuticals

StrengthLooks likeImprint
2 mg / 0.5 mg naloxone hydrochloride dihydrateorange round tablet, 6 mm54 122
8 mg / 2 mg naloxone hydrochloride dihydrateorange round tablet, 10 mm54 375

Source: DailyMed (U.S. National Library of Medicine), from each maker’s FDA drug listing. A few makers are shown, not every one. Never take a pill you can’t identify; ask a pharmacist.

Industry payments about this drug

Drug makers reported $2.6M in payments to clinicians that named this drug in 2025 (meals, speaking, consulting and similar).

  • Braeburn Inc. $1.7M
  • Indivior Inc. $926,261

See all companies →

Source: CMS Open Payments, general payments (not research), program year 2025. A payment is not evidence of wrongdoing. Payments by doctor

Recalls and shortages

Not on the FDA drug shortage list.

3 recalls since 2020

  • Aug 2026 · American Health PAckaging · Class III
    Labeling: Label Mix-up
  • May 2023 · Sun Pharmaceutical Industries Inc · Class II
    CGMP Deviations
  • Sep 2020 · Teva Pharmaceuticals USA · Class II
    Failed Stability Specifications: Below specification result for buprenorphine release rate.

See all recalls →

Recalls usually affect specific lots from one maker, not every version of a drug. Class I is the most serious; most drug recalls are Class II. FDA recalls (opens in a new tab)

Industry-funded trials

Sources: CMS Medicare Part D Prescribers by Provider and Drug (2024; prescriptions include refills, and CMS hides counts under 11 per prescriber); U.S. Food and Drug Administration, openFDA (drug labels, NDC directory, enforcement reports, drug shortages); CMS Open Payments 2025; ClinicalTrials.gov. General information only, not medical advice; not yet reviewed by our medical reviewer.