FDA Orange Book · active-ingredient family
Suzetrigine
Suzetrigine is approved in 1 FDA application, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.
Reference-listed drug:JOURNAVX · NDA 219209
1
Brand (NDA)
0
Generics (ANDA)
1
Listed patents
1
Exclusivity periods
Brand (NDA) products · tablet
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| JOURNAVXRLD | VERTEX PHARMS INC | NDA 219209 | — | Jan 30, 2025 |
Marketing exclusivity (1)
- NCENew chemical entity exclusivity (5 years)
Jan 30, 2030
in 3 yr 8 mo
Listed patents (1)
| Patent | Expires | In | Type |
|---|---|---|---|
| 11834441 | Dec 04, 2040 | in 14 yr 8 mo | SubstanceProductU-4125 |
Suzetrigine — frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

