BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
| Brand name | ZUBSOLV |
|---|---|
| Active ingredient | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
| Strength | EQ 0.7MG BASE;EQ 0.18MG BASE |
| Dosage form | TABLET |
| Route | SUBLINGUAL |
| Modality | Small molecule |
| FDA approval | October 2016 |
| Marketing status | RX |
| Patent | Expires | Type |
|---|---|---|
| 11020388 | September 2032 | product |
| 10946010 | September 2032 | product |
| 9259421 | September 2032 | product |
| 8940330 | September 2032 | product |
| 8470361 | May 2030 | product |
| 8658198 | December 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.