Assyro AI

Orange Book product · Brand (NDA)

TRIUMEQ PD

ABACAVIR SULFATE; DOLUTEGRAVIR SODIUM; LAMIVUDINE

Brand (NDA)NDA 215413RX VIIV HLTHCARE

At a glance

Mar 30, 2022

Approved

Brand (NDA)

Application

Not listed

TE code

4

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Mar 30, 2022

    4 yr 3 mo ago

  2. Exclusivity ends · NPP

    New patient population 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 60MG BASE;EQ 5MG BASE;30MG

Dosage form

TABLET, FOR SUSPENSION

Route

ORAL

TE code

Not listed

Application

NDA 215413

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)

  • NPPNew patient population 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.