Buprenorphine 1.4mg / Naloxone 360microgram sublingual tablets sugar free
Requires a prescription from a doctor or prescriber
Some safe custody exemptions; written records required
Legal requirements and restrictions
Medicines with lower misuse potential than Schedule 2. Subject to special prescription requirements but reduced record-keeping.
Legal requirements
- Safe custody requirements apply (locked storage)
- No controlled drugs register required
- Prescriptions valid for 28 days
- Can be emergency supplied by pharmacists
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Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
Yellow Card
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Drug safety updates
MHRA alerts for Buprenorphine + Naloxone
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Submit a Yellow Card report to the MHRA
Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
MHRA licensed products
View all licensed products for Buprenorphine + Naloxone on the MHRA register
Zubsolv 1.4mg/0.36mg sublingual tablets
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. Contains public sector information licensed under the Open Government Licence v3.0.
WHO defined daily dose (DDD)
8 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(2)
Drug misuse in over 16s: opioid detoxification (CG52)
Opioid dependence: buprenorphine prolonged-release injection (Buvidal) (ES19)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 13 · Randomised trials: 36 · 2011–2026
Showing the 50 most relevant studies, sorted by most relevant.
Joshua D. Lee, E. Nunes, Patricia Novo, et al.
Lancet (London, England), 2017
- Opioid-Related Disorders
- Substance Withdrawal Syndrome
- Naltrexone
L. Tanum, K. Solli, Zill-E-Huma Latif, et al.
JAMA Psychiatry, 2017
G. D'Onofrio, P. O'Connor, M. Pantalon, et al.
JAMA, 2015
S. Weiss, H. Douglas
Journal of Addiction Medicine, 2020
Pereira da Silva AM, de Bastos Maximiano ML, Cabeça LS, et al.
2026
- Opioid-Related Disorders
- Methadone
- Narcotic Antagonists
Enns B, Guerra-Alejos BC, Min JE, et al.
2025
- Opioid-Related Disorders
- Methadone
- Opiate Substitution Treatment
ImportanceIn 2017, British Columbia guidelines changed the preferred first-line treatment for opioid use disorder from methadone to buprenorphine/naloxone. Systematic reviews have consistently shown better treatment retention associated with methadone, while studies have reported a reduced risk of mortality associated with buprenorphine/naloxone, causing confusion in interpretation for clinical guidelines.ObjectiveTo estimate the population-level health benefits and harms associated with buprenorphine/naloxone vs methadone for treatment of opioid use disorder, accounting for differences in treatment retention and risk of mortality while receiving treatment.Design, setting, and participantsThis decision analytic model analysis was conducted from January 1, 2010, to March 17, 2020, using a semi-Markov cohort model and linked population-level health administrative data on all individuals presenting for opioid agonist treatment in British Columbia, Canada. Hazard ratios were estimated for the association of buprenorphine/naloxone vs methadone with treatment discontinuation (breaks in dispensations lasting ≥5 days for methadone and ≥6 days for buprenorphine/naloxone) and mortality while receiving treatment (per protocol). Treatment episodes in primary analysis were based on the medication initiated (initiator analysis). Probabilistic (mean estimates and 95% credible intervals from 10 000 simulations) and deterministic sensitivity analyses were conducted. Data were analyzed between August 2023 and October 2024.ExposureAlternative treatment policies in which buprenorphine/naloxone or methadone were exclusively available to individuals presenting for opioid agonist treatment.Main outcome and measuresIncremental life-years, fatal overdoses, and all-cause deaths.ResultsThe study population included 40 461 individuals with 109 126 cumulative person-years of follow-up (median [IQR] age, 33 [23-43] years; 66.0% [range, 56.0%-76.0%] male). A policy of exclusively buprenorphine/naloxone was estimated to have -1602 incremental life-years (95% credible interval, -3249 to -549 life-years) compared with methadone, with an additional 221 fatal overdoses (95% credible interval, 119 to 376 overdoses) and 303 all-cause deaths (95% credible interval, 120 to 589 deaths) over a 10-year period.Conclusions and relevanceResults from this study suggest that any advantages from a reduced risk of mortality with treatment with buprenorphine/naloxone were outweighed by deficits in treatment retention. Evaluated in a jurisdiction where both medications were available in office-based settings, these findings do not support recommendations of buprenorphine/naloxone as first-line treatment over methadone.
Abstract licence: CC BY
Awaji BH, Abanmi SN, Alqahtani MS, et al.
2025
Michael A. Yokell, Nickolas D. Zaller, Traci C. Green, et al.
Current Drug Abuse Reviewse, 2011
M. Piske, T. Thomson, E. Krebs, et al.
BMJ Open, 2020
Y. Hser, Elizabeth Evans, David Y. C. Huang, et al.
Addiction (Abingdon, England), 2016
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.