Assyro AI

Orange Book product · Brand (NDA)

TRIUMEQ

ABACAVIR SULFATE; DOLUTEGRAVIR SODIUM; LAMIVUDINE

Brand (NDA)NDA 205551RX VIIV HLTHCARE

At a glance

Aug 22, 2014

Approved

Brand (NDA)

Application

Not listed

TE code

4

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Aug 22, 2014

    12 yr ago

  2. Exclusivity ends · M-294

    New use / labeling-change exclusivity (3 years)

    Jun 15, 2026

    4 d ago

  3. Today

  4. Exclusivity ends · PED

    Pediatric exclusivity (adds 6 months)

    Dec 15, 2026

    in 6 mo

  5. Patent 8129385 expires

    Listed drug substance patent expiration.

    Oct 05, 2027

    in 1 yr 4 mo

  6. Patent 8129385*PED expires

    Listed listed patent expiration.

    Apr 05, 2028

    in 1 yr 10 mo

  7. Patent 9242986 expires

    Listed drug substance patent expiration.

    Dec 08, 2029

    in 3 yr 6 mo

  8. Patent 9242986*PED expires

    Listed listed patent expiration.

    Jun 08, 2030

    in 4 yr

Pharmaceutical detail

Active ingredient

ABACAVIR SULFATE; DOLUTEGRAVIR SODIUM; LAMIVUDINE

Strength

EQ 600MG BASE;EQ 50MG BASE;300MG

Dosage form

TABLET

Route

ORAL

TE code

Not listed

Application

NDA 205551

Product number

001

Marketing status

RX

Reference listed drug (RLD)

Yes

Reference standard (RS)

Yes

Active-ingredient family

View full family

This is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.

Marketing exclusivity (2)

  • M-294New use / labeling-change exclusivity (3 years)

    Jun 15, 2026

    4 d ago

  • PEDPediatric exclusivity (adds 6 months)

    Dec 15, 2026

    in 6 mo

Listed patents (4)

Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
8129385Oct 05, 2027in 1 yr 4 mo
SubstanceProduct
8129385*PEDApr 05, 2028in 1 yr 10 mo
9242986Dec 08, 2029in 3 yr 6 mo
SubstanceProduct
9242986*PEDJun 08, 2030in 4 yr
Agent CTA Background

Your Next Submission Could Take 6+ Fewer Weeks and Cost $250K Less.