United States· US:0024-5761_dd3cca75-32f2-4e6d-8121-20f47e101495

Soliqua 100/33

A insulin glargine and lixisenatide product containing insulin glargine; lixisenatide, registered in United States by Sanofi-Aventis U.S. LLC. The same ATC class is registered in 10 of our 19 countries.

ATC A10AE54US label

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedSoliqua 100/33ATCA10AE54REGISTER NO.US:0024-5761_dd3cca75…PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Insulin glargine and lixisenatide is registered in 10 of 19 countries.

Countries holding a registration under ATC A10AE54 (insulin glargine and lixisenatide), each read from that country’s own register.

  • This record: United States, from FDA National Drug Code directory (United States)
  • 6 of them publish a price we can compare per daily dose

Insulin glargine and lixisenatide · ATC A10AE54

10 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Netherlands
  • Polandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
INSULIN GLARGINE; LIXISENATIDE
Manufacturer
Sanofi-Aventis U.S. LLC
Country
United States (US)
ATC code
A10AE54
ATC class
Insulin glargine and lixisenatide
Defined daily dose
40 E, P
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    0024-5761-01
  • ndc11
    0024-5761-05

Regulatory notes

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

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/d9cad7be-d27a-4edb-b4e4-4a09e0cddab7
GET /v1/drugs/d9cad7be-d27a-4edb-b4e4-4a09e0cddab7?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": "SUBCUTANEOUS",
  "source": "ndc",
  "strength": "100; 33",
  "substance": "INSULIN GLARGINE; LIXISENATIDE",
  "productndc": "0024-5761",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "U/mL; ug/mL",
  "application_number": "BLA208673",
  "marketing_category": "BLA"
}

See everything about insulin glargine and lixisenatide.

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.