MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE
| Brand name | EMBEDA |
|---|---|
| Active ingredient | MORPHINE SULFATE; NALTREXONE HYDROCHLORIDE |
| Strength | 30MG;1.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Dosage form | CAPSULE, EXTENDED RELEASE |
| Route | ORAL |
| Modality | Small molecule |
| FDA approval | August 2009 |
| Marketing status | DISCN |
| Patent | Expires | Type |
|---|---|---|
| 8623418 | November 2029 | use U-1640 |
| 7815934 | December 2027 | product |
| 7682633 | June 2027 | use U-1510 |
| 7682634 | June 2027 | product |
| 8877247 | June 2027 | product |
| 8846104 | June 2027 | product |
| 8158156 | June 2027 | use U-1510 |
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.