FDA Orange Book · active-ingredient family
Cabotegravir sodium
Cabotegravir sodium is approved in 1 FDA application, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.
Reference-listed drug:VOCABRIA · NDA 212887
1
Brand (NDA)
0
Generics (ANDA)
2
Listed patents
1
Exclusivity periods
Brand (NDA) products · tablet
| Product | Applicant | Application | TE | Approved | |
|---|---|---|---|---|---|
| VOCABRIARLD | VIIV HLTHCARE | NDA 212887 | — | Jan 21, 2021 |
Marketing exclusivity (1)
- NCENew chemical entity exclusivity (5 years)
Jan 21, 2026
5 mo ago
Listed patents (2)
| Patent | Expires | In | Type |
|---|---|---|---|
| 10927129 | Apr 28, 2026 | 2 mo ago | SubstanceProduct |
| 8410103 | Feb 04, 2031 | in 4 yr 8 mo | SubstanceProductU-3348 |
Cabotegravir sodium — frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

