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Are They Discontinuing Buprenorphine? The Status of OUD Medication in 2025

4 min read

In 2022, an estimated 9.3 million U.S. adults needed treatment for opioid use disorder (OUD), but only 25.1% received medications for it [1.6.4]. Amid this crisis, many ask: are they discontinuing buprenorphine, a key medication for OUD?

Quick Summary

Buprenorphine as a generic medication is not being discontinued and remains a vital treatment. However, specific brand-name formulations like Subutex and Suboxone tablets have been discontinued for various reasons.

Key Points

  • Not Discontinued: The generic medication buprenorphine is not being discontinued and remains a key treatment for Opioid Use Disorder (OUD) [1.3.2, 1.3.3].

  • Brand Name vs. Generic: Confusion arises because specific brand names like Subutex and Suboxone tablets have been discontinued, but their generic versions remain available [1.2.2, 1.4.4].

  • Safety Formulations: Many combination products (e.g., Suboxone film) include naloxone to deter misuse through injection, a key reason manufacturers shifted away from older tablet forms [1.2.3, 1.8.1].

  • Access is the Real Issue: The primary problem is not discontinuation but significant barriers to access, including pharmacy availability, provider shortages, and regulatory hurdles [1.5.1, 1.5.2].

  • Various Formulations Exist: Buprenorphine is available in many forms, including sublingual films/tablets, monthly injections, and buccal films, to suit different patient needs [1.7.3].

  • Discontinuations for Market Reasons: Past discontinuations of brands like Subutex (2011) and Probuphine (2020) were cited as being for market or safety alternative reasons, not a lack of effectiveness [1.2.3, 1.7.3].

  • Ongoing Availability Issues: In 2025, patients continue to face availability issues due to supply chain disruptions, manufacturing bottlenecks, and policy delays impacting telemedicine [1.5.1].

In This Article

The Current State of Buprenorphine Availability

Buprenorphine is a critical medication used in the treatment of Opioid Use Disorder (OUD). Contrary to some rumors, the generic medication buprenorphine is not being discontinued [1.3.2, 1.3.3]. It remains a cornerstone of Medication-Assisted Treatment (MAT) and is on the World Health Organization's list of essential medications [1.7.5]. However, the confusion often arises from the discontinuation of specific brand-name products containing buprenorphine. For instance, the brand Subutex, a buprenorphine-only tablet, was discontinued by its manufacturer in 2011, citing the availability of safer alternatives [1.2.3, 1.2.4]. Similarly, brand-name Suboxone tablets (a combination of buprenorphine and naloxone) were voluntarily discontinued by the manufacturer in 2012 due to concerns about higher rates of accidental pediatric exposure compared to the film version [1.4.2, 1.4.3]. The FDA has determined that these products were not withdrawn for reasons of safety or effectiveness, which allows for the continued approval and sale of generic versions [1.3.3, 1.3.4].

Understanding Buprenorphine and Its Formulations

Buprenorphine is a partial opioid agonist. This means it binds to and activates opioid receptors in the brain, but to a lesser degree than full agonists like heroin or fentanyl [1.7.3]. This action helps to reduce cravings and withdrawal symptoms without producing the same intense high, and it has a "ceiling effect" that lowers the risk of respiratory depression at higher doses [1.7.3, 1.7.5].

There are two primary types of buprenorphine medications:

  • Buprenorphine-only (Monotherapy): Originally marketed as Subutex, this form is still available as a generic. It's often used in supervised medical settings, such as during the initial phase of treatment (induction), or for patients who cannot tolerate naloxone, like pregnant individuals [1.2.3, 1.8.3].
  • Buprenorphine/Naloxone Combination: The most common brand name is Suboxone. This formulation includes naloxone, an opioid antagonist. When taken as prescribed (sublingually), the naloxone has negligible effect. However, if the medication is crushed and injected, the naloxone becomes active and can cause immediate, unpleasant withdrawal symptoms. This mechanism is designed to deter misuse and diversion [1.2.2, 1.8.5].

Buprenorphine is available in various forms to meet different patient needs:

  • Sublingual Films & Tablets: Dissolve under the tongue (Suboxone, Zubsolv, generics) [1.7.2].
  • Buccal Films: Dissolve on the inside of the cheek (Belbuca) [1.7.3].
  • Extended-Release Injections: Administered monthly by a healthcare provider (Sublocade) [1.7.3].
  • Transdermal Patches: Applied to the skin for chronic pain management (Butrans) [1.7.3].
  • Subdermal Implants: While Probuphine® was a six-month implant, it was discontinued in 2020 for commercial reasons, not safety [1.7.3].

Challenges to Access in 2025

Despite the continued availability of generic buprenorphine, patients face significant hurdles in accessing the medication in 2025. These are not due to a wholesale discontinuation but rather a complex web of systemic issues.

Recent studies from September 2025 show that only about 2 in 5 retail pharmacies carried buprenorphine in 2023 [1.5.4]. Access is particularly limited in rural areas and in neighborhoods with predominantly Black or Latino populations [1.5.2]. Reasons for these access barriers include:

  • Regulatory & Policy Delays: The DEA and HHS have delayed the implementation of new rules for prescribing buprenorphine via telemedicine until late 2025, creating uncertainty for providers [1.5.1, 1.5.5].
  • Manufacturing & Supply Chain Issues: Shortages of raw materials and stricter quality control protocols, partly in response to lawsuits concerning dental issues with film formulations, have created manufacturing bottlenecks [1.5.1].
  • Provider Shortages: A lack of healthcare providers authorized and willing to prescribe buprenorphine, especially in rural counties, remains a major barrier [1.5.1, 1.5.2].
  • Pharmacy-Level Barriers: Some pharmacies are unwilling to stock the medication, creating so-called "pharmacy deserts" for OUD treatment [1.5.2, 1.5.3].

Buprenorphine vs. Buprenorphine/Naloxone Comparison

Feature Buprenorphine-Only (e.g., generic Subutex) Buprenorphine/Naloxone (e.g., Suboxone)
Ingredients Buprenorphine [1.2.3] Buprenorphine + Naloxone [1.2.3]
Abuse Deterrent No naloxone safeguard against injection abuse [1.2.3]. Naloxone included to precipitate withdrawal if injected, deterring misuse [1.8.1].
Common Use Cases Induction phase of treatment, pregnant patients, or those with a naloxone allergy [1.2.3]. Standard for outpatient and long-term maintenance treatment [1.2.3, 1.8.4].
Formulations Generic sublingual tablets, some long-acting injections (Sublocade) [1.2.3, 1.7.3]. Sublingual films, sublingual tablets, buccal films [1.7.2].
Brand Status The brand name Subutex was discontinued in 2011 [1.2.2]. Brand name Suboxone tablets were discontinued in 2012, but films and generics are available [1.4.4, 1.4.5].

Conclusion

To directly answer the question: no, they are not discontinuing buprenorphine as a medication. It is an essential, life-saving drug for opioid use disorder that remains available, primarily in generic forms. The narrative of discontinuation stems from business decisions by manufacturers to stop producing specific brand-name products, like Subutex and Suboxone tablets, often in favor of formulations considered safer or less prone to misuse [1.2.3, 1.4.2]. The real crisis is not a discontinuation of the drug itself, but rather the persistent and complex barriers—from manufacturing and regulations to provider and pharmacy availability—that prevent this vital medication from reaching many of the millions who need it [1.5.1, 1.6.4]. The focus for patients, providers, and policymakers should be on dismantling these barriers to improve access to treatment.


Authoritative Link: Substance Abuse and Mental Health Services Administration (SAMHSA) - Buprenorphine

Frequently Asked Questions

The manufacturer discontinued the brand name Subutex in the U.S. in 2011, citing the development of safer formulations like Suboxone (which contains naloxone) that are less likely to be misused or diverted [1.2.2, 1.2.3].

The brand-name Suboxone tablets were discontinued by the manufacturer in 2012 due to a higher risk of accidental pediatric exposure compared to the film version. However, generic buprenorphine/naloxone tablets are still available [1.4.2, 1.4.4].

No, buprenorphine formulations for pain, such as the Butrans transdermal patch and Belbuca buccal film, are not being discontinued, though individual patient decisions to stop using them can be influenced by various factors [1.9.1, 1.10.3].

Buprenorphine is the active medication. Suboxone is a brand name for a combination product that contains both buprenorphine and naloxone. The naloxone is added to deter misuse by injection [1.2.3, 1.8.3].

Yes, buprenorphine is still available by prescription. It can be prescribed by qualified healthcare providers for the treatment of opioid use disorder and for pain management, although some patients face access issues [1.5.1, 1.5.2].

Yes, there are reports of buprenorphine availability issues in 2025. These are caused by manufacturing bottlenecks, raw material shortages, and disruptions in the supply chain, rather than an official discontinuation of the drug [1.5.1].

If a specific brand is discontinued or unavailable, there are often generic equivalents or different formulations (e.g., film instead of tablet, or an injectable like Sublocade) that your doctor can prescribe. It is important to discuss these options with your healthcare provider [1.2.2, 1.7.3].

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.