Drug facts

Brand

Triumeq (Abacavir, Dolutegravir and Lamivudine)

No generic abacavir, dolutegravir and lamivudine is approved; the latest Triumeq patent or exclusivity in the Orange Book runs to 06/08/2030. 6 staged generic applications passed FDA review and wait on patents or exclusivity.

Triumeq was first approved by the FDA on 08/22/2014 under NDA 205551; the application holder is Viiv Healthcare Co.

The latest NADAC for TRIUMEQ 600-50-300 MG TABLET is $130.08 per unit (as of 10/28/2026).

Holder Viiv Healthcare CoApplication NDA 205551Approved 08/22/2014

01Patents and exclusivity

When competition can legally begin. A generic can launch once both exclusivity and the last listed patent expire, unless a court or settlement says otherwise.

1,316days until the latest patent expires

ExclusivityPatent onlyOpen to generics
Today
Approved08/22/2014
Exclusivity ends12/15/2026
Last patent06/08/2030
201520182021202420272030
Latest patent
06/08/2030Triumeq
Orange Book
Exclusivity
12/15/2026Triumeq
Orange Book

02Competition

Generics
No generic approved
Orange Book
Staged generics
6 passed FDA review, awaiting market entry
FDA
Every listingEach listing and maker behind the generics count.
Price erosionHow NADAC moves as generics enter.
PrescribersWho prescribes it, from Medicare data.
Available in the full Triumeq profile.See what is included

03Supply and price

FDA drug shortage
ClearNot on the current shortage list
FDA shortages
NADAC
$130.08 per unitTRIUMEQ 600-50-300 MG TABLET, as of 10/28/2026
CMS NADAC

04Product

Application holder
Viiv Healthcare Co
Orange Book
Application
NDA 205551
Orange Book
First approved
08/22/2014
Orange Book
Dosage forms
tablet
Routes
oral
Other brand names
Triumeq Pd

Sources: FDA Orange Book, FDA Purple Book, FDA drug shortages, FDA enforcement reports and CMS NADAC, read through QOPE. Not medical or legal advice.