AMIODARONE HYDROCHLORIDE
| Brand name | NEXTERONE |
|---|---|
| Active ingredient | AMIODARONE HYDROCHLORIDE |
| Strength | 150MG/100ML (1.5MG/ML) |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Modality | Small molecule |
| FDA approval | November 2010 |
| Marketing status | RX |
| Patent | Expires | Type |
|---|---|---|
| 9493582 | February 2033 | product |
| 10117951 | March 2029 | product |
| 8410077 | March 2029 | product |
| 7635773 | March 2029 | product |
| 9200088 | March 2029 | product |
| 9750822 | March 2029 | product |
| 10177951 | March 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.