FDA Orange Book · active-ingredient family
Fosdenopterin hydrobromide
Fosdenopterin hydrobromide is approved in 1 FDA application, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.
Reference-listed drug:NULIBRY · NDA 214018
1
Brand (NDA)
0
Generics (ANDA)
1
Listed patents
2
Exclusivity periods
Brand (NDA) products · powder
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| NULIBRYRLD | SENTYNL THERAPS INC | NDA 214018 | — | Feb 26, 2021 |
Marketing exclusivity (2)
- NCENew chemical entity exclusivity (5 years)
Feb 26, 2026
4 mo ago
- ODE-342Orphan-drug exclusivity (7 years)
Feb 26, 2028
in 1 yr 9 mo
Listed patents (1)
| Patent | Expires | In | Type |
|---|---|---|---|
| 7504095 | Apr 09, 2029 | in 2 yr 10 mo | ProductU-3092 |
Fosdenopterin hydrobromide — frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

