NALOXONE HYDROCHLORIDE
| Brand name | ZIMHI |
|---|---|
| Active ingredient | NALOXONE HYDROCHLORIDE |
| Strength | 5MG/0.5ML (5MG/0.5ML) |
| Dosage form | SOLUTION |
| Route | INTRAMUSCULAR, SUBCUTANEOUS |
| Modality | Small molecule |
| FDA approval | October 2021 |
| Marketing status | RX |
| Patent | Expires | Type |
|---|---|---|
| 11571518 | June 2041 | product |
| 11027072 | May 2039 | 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.