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Belgium· BE-AMP-SAM663878-00

Eylea 114.3 mg/ml

A aflibercept product containing aflibercept, registered in Belgium by Bayer. The same ATC class is registered in 11 of our 19 countries.

ATC S01LA05

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedEylea 114.3 mg/mlATCS01LA05REGISTER NO.BE-AMP-SAM663878-00PACKS LISTED1CHECKEDSeptember 26, 2026

Where it is registered

Aflibercept is registered in 11 of 19 countries.

Countries holding a registration under ATC S01LA05 (aflibercept), each read from that country’s own register.

  • This record: Belgium, from FAMHP / AFMPS (Belgium)
  • 7 of them publish a price we can compare per daily dose

Aflibercept · ATC S01LA05

11 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
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

FAMHP / AFMPS (Belgium)
Active substance
Aflibercept
Manufacturer
Bayer
Country
Belgium (BE)
ATC code
S01LA05
ATC class
Aflibercept
Defined daily dose
0.018 DE, IVT
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 1

  • be_apb
    7748502

Regulatory notes

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

Same medicine, other countries

Aflibercept in 15 other countries

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

All aflibercept products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • United Kingdom (Northern Ireland) · Vgenfli
  • Iceland · Afiveg, Afqlir
  • Liechtenstein · Afiveg, Afqlir
  • Norway · Afiveg, Afqlir

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FAMHP / AFMPS (Belgium). 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/19f3d924-4fd6-4eb1-a2d2-82455647ed9c
GET /v1/drugs/19f3d924-4fd6-4eb1-a2d2-82455647ed9c?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.

{
  "form": "Solution for injection in pre-filled syringe",
  "source": "afmps",
  "status": "AUTHORIZED",
  "name_en": "Eylea 114.3 mg/ml",
  "name_fr": "Eylea 114.3 mg/ml",
  "name_nl": "Eylea 114.3 mg/ml",
  "amp_code": "SAM663878-00",
  "strengths": [
    "114.3000",
    "114.3000"
  ],
  "pack_count": 1,
  "substances": [
    "Aflibercept",
    "Sucrose",
    "Polysorbate 20"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Aflibercept",
  "authorisation_numbers": [
    "EU/1/12/797/004"
  ]
}

See everything about aflibercept.

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.