26 authorised products containing Buprenorphine hydrochloride, from the HPRA register.
| Medicine | Active substance | Licence holder | Status |
|---|---|---|---|
| Bulexin 2 mg/0.5 mg sublingual tablets PA0281/267/001 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Pinewood Laboratories Limited | Marketed |
| Bulexin 4 mg/1 mg sublingual tablets PA0281/267/002 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Pinewood Laboratories Limited | Not marketed |
| Bulexin 8 mg/2 mg sublingual tablets PA0281/267/003 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Pinewood Laboratories Limited | Marketed |
| Buprenorphine 0.4 mg Sublingual Tablets PA1567/001/001 |
Buprenorphine hydrochloride | Activase Pharmaceuticals Limited | Not marketed |
| Buprenorphine 2 mg Sublingual Tablets PA23142/003/001 |
Buprenorphine hydrochloride | Aspire Pharma (Malta) Limited | Not marketed |
| Buprenorphine 2 mg Sublingual Tablets PA1567/001/002 |
Buprenorphine hydrochloride | Activase Pharmaceuticals Limited | Not marketed |
| Buprenorphine 8 mg Sublingual Tablets PA23142/003/002 |
Buprenorphine hydrochloride | Aspire Pharma (Malta) Limited | Not marketed |
| Buprenorphine 8 mg Sublingual Tablets PA1567/001/003 |
Buprenorphine hydrochloride | Activase Pharmaceuticals Limited | Not marketed |
| Buprenorphine Neuraxpharm EU/1/24/1809/001-003 |
Buprenorphine hydrochloride | Laboratorios Lesvi, S.L. | — |
| Buprenorphine Neuraxpharm EU/1/24/1809/004-006 |
Buprenorphine hydrochloride | Laboratorios Lesvi, S.L. | — |
| Buprenorphine Neuraxpharm EU/1/24/1809/007-009 |
Buprenorphine hydrochloride | Laboratorios Lesvi, S.L. | — |
| Buprenorphine Neuraxpharm EU/1/24/1809/010-012 |
Buprenorphine hydrochloride | Laboratorios Lesvi, S.L. | — |
| Suboxone 12 mg/3 mg Sublingual film EU/1/06/359/016-018 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Indivior Europe Limited | — |
| Suboxone 16 mg/4 mg Sublingual tablet EU/1/06/359/005-006 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Indivior Europe Limited | — |
| Suboxone 2 mg/0.5 mg Sublingual film EU/1/06/359/007-009 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Indivior Europe Limited | — |
| Suboxone 4 mg/1 mg Sublingual film EU/1/06/359/010-012 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Indivior Europe Limited | — |
| Suboxone 8 mg/2 mg Sublingual film EU/1/06/359/013-015 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Indivior Europe Limited | — |
| Suboxone 8 mg/2 mg Sublingual tablet EU/1/06/359/03-04 |
Buprenorphine hydrochloride, NALOXONE HYDROCHLORIDE | Indivior Europe Limited | — |
| Temgesic 200 microgram Sublingual Tablets PA23460/001/001 |
Buprenorphine hydrochloride | Eumedica Pharmaceuticals GmbH | Not marketed |
| Temgesic 300 micrograms/ml, solution for injection PA23460/001/002 |
Buprenorphine hydrochloride | Eumedica Pharmaceuticals GmbH | Not marketed |
| Zubsolv 0.7 mg/0.18 mg Sublingual tablet EU/1/17/1233/001 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Accord Healthcare S.L.U. | — |
| Zubsolv 1.4 mg/0.36 mg sublingual tablets EU/1/17/1233/002 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Accord Healthcare S.L.U. | — |
| Zubsolv 11.4 mg/2.9 mg Sublingual tablet EU/1/17/1233/006 |
Naloxone hydrochloride dihydrate, Buprenorphine hydrochloride | Accord Healthcare S.L.U. | — |
| Zubsolv 2.9 mg/0.71 mg Sublingual tablet EU/1/17/1233/003 |
Naloxone hydrochloride dihydrate, Buprenorphine hydrochloride | Accord Healthcare S.L.U. | — |
| Zubsolv 5.7 mg/1.4 mg Sublingual tablet EU/1/17/1233/004 |
Naloxone hydrochloride dihydrate, Buprenorphine hydrochloride | Accord Healthcare S.L.U. | — |
| Zubsolv 8.6 mg/2.1 mg Sublingual tablet EU/1/17/1233/005 |
Buprenorphine hydrochloride, Naloxone hydrochloride dihydrate | Accord Healthcare S.L.U. | — |
Priya Life Science (2026). Irish Medicines Database. Available at: https://priyalifescience.com/medicines (Accessed: 13 August 2026).
Data: Health Products Regulatory Authority (HPRA) open dataset (“Authorised or Transfer Pending Products”), licensed CC BY 4.0, refreshed daily. Regulatory information only — not medical advice.