BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
| Brand name | SUBOXONE |
|---|---|
| Active ingredient | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
| Strength | EQ 8MG BASE;EQ 2MG BASE |
| Dosage form | FILM |
| Route | BUCCAL, SUBLINGUAL |
| Modality | Small molecule |
| FDA approval | August 2010 |
| Marketing status | RX |
| Patent | Expires | Type |
|---|---|---|
| 8475832 | March 2030 | product |
| 9687454 | August 2029 | product |
| 11135216 | August 2029 | product |
Source: FDA Orange Book, layered on the CliffBio company graph. Cliff dates are the latest FDA-listed patent expiry; estimates are projections, not legal advice.