FDA Orange Book · active-ingredient family
Golodirsen
Golodirsen is approved in 1 FDA application, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.
Reference-listed drug:VYONDYS 53 · NDA 211970
1
Brand (NDA)
0
Generics (ANDA)
1
Listed patents
1
Exclusivity periods
Brand (NDA) products · solution
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| VYONDYS 53RLD | SAREPTA THERAPS INC | NDA 211970 | — | Dec 12, 2019 |
Marketing exclusivity (1)
- ODE-280Orphan-drug exclusivity (7 years)
Dec 12, 2026
in 6 mo
Listed patents (1)
| Patent | Expires | In | Type |
|---|---|---|---|
| RE47691 | Jun 28, 2028 | in 2 yr 1 mo | Product |
Golodirsen — frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

