AMIODARONE HYDROCHLORIDE
| Brand name | NEXTERONE |
|---|---|
| Active ingredient | AMIODARONE HYDROCHLORIDE |
| Strength | 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Modality | Small molecule |
| FDA approval | December 2008 |
| Marketing status | DISCN |
| Patent | Expires | Type |
|---|---|---|
| 7635773 | 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.