NALOXONE HYDROCHLORIDE
| Brand name | NALOXONE HYDROCHLORIDE (AUTOINJECTOR) |
|---|---|
| Active ingredient | NALOXONE HYDROCHLORIDE |
| Strength | 10MG/0.4ML (10MG/0.4ML) |
| Dosage form | SOLUTION |
| Route | INTRAMUSCULAR, SUBCUTANEOUS |
| Modality | Small molecule |
| FDA approval | February 2022 |
| Marketing status | DISCN |
| Patent | Expires | Type |
|---|---|---|
| 10143792 | May 2031 | use U-2476 |
| 10322239 | February 2031 | use U-1907 |
| 9474869 | February 2031 | product |
| 8939943 | February 2031 | product |
| 9022022 | February 2031 | product |
| 9814838 | February 2031 | 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.