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Netherlands· NL-f0df2a9b7bcc

Simponi 45 mg/0.45 mL oplossing voor injectie in voorgevulde pen

A golimumab product containing golimumab, registered in Netherlands by Janssen-Cilag International NV. The same ATC class is registered in 14 of our 19 countries.

ATC L04AB06

Checked against CBG-MEB (Netherlands) on

Informational only — not a medical device.

SOURCE REGISTER · NLCBG-MEB (Netherlands)normalisedSimponi 45 mg/0.45 mL oplossing voor …ATCL04AB06REGISTER NO.NL-f0df2a9b7bccPACKS LISTED1CHECKEDSeptember 29, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about golimumabAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Golimumab is registered in 14 of 19 countries.

Countries holding a registration under ATC L04AB06 (golimumab), each read from that country’s own register.

  • This record: Netherlands, from CBG-MEB (Netherlands)
  • 9 of them publish a price we can compare per daily dose
Search golimumab products by name

Golimumab · ATC L04AB06

14 / 19 countries

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

CBG-MEB (Netherlands)
Active substance
GOLIMUMAB
Manufacturer
Janssen-Cilag International NV
Country
Netherlands (NL)
ATC code
L04AB06
ATC class
Golimumab
Defined daily dose
1.66 mg, P
Reimbursed
Not published by this register
Source register
CBG-MEB (Netherlands)
Last checked
September 29, 2026

Packs & prices · 1

  • cbg_meb_id
    EU/1/09/546

Regulatory notes

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

Interactions

429 interactions on record for golimumab.

Graded by severity as the source publishes them — 287 severe. Severity grades are free for everyone; mechanism and management come with Growth.

  • Severity for every pair — free, no plan needed
  • The source, licence and sync date on every record
  • Mechanism and what to do for each pair — Growth plan
Check golimumab against other medicinesHow interaction checks work

Golimumab · interactions on record

429 records

  • 287 severe
  • 135 moderate
  • 7 minor

Most severe, free to view

  • PrednisoloneA07EA01severe
  • HydrocortisoneA07EA02severe
  • PrednisoneA07EA03severe
  • BetamethasoneA07EA04severe
  • Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Golimumab in 15 other countries

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

All golimumab products

Authorised across Europe · EMA

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

  • United Kingdom (Northern Ireland) · Gotenfia
  • Iceland · Gobivaz, Gotenfia
  • Liechtenstein · Gobivaz, Gotenfia
  • Norway · Gobivaz, Gotenfia

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 CBG-MEB (Netherlands). 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/a85d4291-4bf5-435c-ab00-dd50585d1b06
GET /v1/drugs/a85d4291-4bf5-435c-ab00-dd50585d1b06?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": "Oplossing voor injectie",
  "route": "Subcutaan gebruik",
  "soort": null,
  "source": "cbg_meb",
  "smpc_url": "https://www.ema.europa.eu/en/documents/product-information/simponi-epar-product-information_nl.pdf",
  "strength": null,
  "atc_label": "Golimumab",
  "detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp123098",
  "excipients": [
    "HISTIDINE, (L-)",
    "HISTIDINEMONOHYDROCHLORIDE 1-WATER (L-)",
    "POLYSORBAAT 80 (E 433)",
    "SORBITOL (E 420)",
    "WATER VOOR INJECTIE"
  ],
  "substances": [
    "GOLIMUMAB"
  ],
  "leaflet_url": null,
  "authorised_at": "2019/02/18",
  "procedure_number": "EMEA/H/C/000992",
  "dispensing_status": "Uitsluitend recept",
  "registration_number": "EU/1/09/546",
  "additional_monitoring": "N"
}
API referenceMCP serverPlans

See everything about golimumab.

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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