BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
| Brand name | BUNAVAIL |
|---|---|
| Active ingredient | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
| Strength | EQ 6.3MG BASE;EQ 1MG BASE |
| Dosage form | FILM |
| Route | BUCCAL |
| Modality | Small molecule |
| FDA approval | June 2014 |
| Marketing status | DISCN |
| Patent | Expires | Type |
|---|---|---|
| 9522188 | April 2035 | product |
| 8703177 | August 2032 | product |
| 9655843 | July 2027 | product |
| 8147866 | July 2027 | 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.