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United States· US:0173-0859_10ccfa0a-0453-41bd-b092-d62863a82c26

Breo Ellipta

A medicinal product containing fluticasone furoate; vilanterol trifenatate, registered in United States by GlaxoSmithKline LLC.

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedBreo ElliptaATC—REGISTER NO.US:0173-0859_10ccfa0a…PACKS LISTED2CHECKEDSeptember 27, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about fluticasone furoate; vilanterol trifenatateAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
FLUTICASONE FUROATE; VILANTEROL TRIFENATATE
Manufacturer
GlaxoSmithKline LLC
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    0173-0859-10
  • ndc11
    0173-0859-14

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Fluticasone furoate; vilanterol trifenatate in 3 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All fluticasone furoate; vilanterol trifenatate products

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/939bed26-0478-4dc4-82ce-37a1649124f1
GET /v1/drugs/939bed26-0478-4dc4-82ce-37a1649124f1?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "RESPIRATORY (INHALATION)",
  "source": "ndc",
  "strength": "100; 25",
  "substance": "FLUTICASONE FUROATE; VILANTEROL TRIFENATATE",
  "productndc": "0173-0859",
  "dosage_form": "POWDER",
  "dea_schedule": null,
  "strength_unit": "ug/1; ug/1",
  "application_number": "NDA204275",
  "marketing_category": "NDA"
}
API referenceMCP serverPlans

See everything about fluticasone furoate; vilanterol trifenatate.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.

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