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France· FR:62975984

HUMIRA 20 mg, solution injectable en seringue préremplie

A adalimumab product containing adalimumab, registered in France by ABBVIE DEUTSCHLAND (ALLEMAGNE), on the national reimbursement list. The same ATC class is registered in 14 of our 19 countries.

Reimbursed in France (Assurance maladie)ATC L04AB04

Checked against Base de données publique des médicaments — BDPM (France) on

Informational only — not a medical device.

SOURCE REGISTER · FRBase de données publique des médicament…normalisedHUMIRA 20 mg, solution injectable en …ATCL04AB04REGISTER NO.FR:62975984PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Adalimumab is registered in 14 of 19 countries.

Countries holding a registration under ATC L04AB04 (adalimumab), each read from that country’s own register.

  • This record: France, from Base de données publique des médicaments — BDPM (France)
  • 9 of them publish a price we can compare per daily dose

Adalimumab · ATC L04AB04

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.

Price per daily dose

What a daily dose of adalimumab costs, country by country.

Normalised to the WHO defined daily dose (2.9 mg), the median price runs from $0.015 in France to $36.00 in Switzerland — a ×2384 gap.

  • France: $0.015 per daily dose (median across products in the class)
  • Public list prices, converted to USD at the rate date shown

Adalimumab · price per daily dose (2.9 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$36.00
  • FR France$0.015
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

Base de données publique des médicaments — BDPM (France)
Active substance
ADALIMUMAB
Manufacturer
ABBVIE DEUTSCHLAND (ALLEMAGNE)
Country
France (FR)
ATC code
L04AB04
ATC class
Adalimumab
Defined daily dose
2.9 mg, P
Reimbursed
Yes
Source register
Base de données publique des médicaments — BDPM (France)
Last checked
September 12, 2026

Packs & prices · 1

1 priced
  • cip13
    3400930126165
    2 seringue(s) préremplie(s) en verre de 0,2 ml avec tampon(s) alcoolisé(s)
    EUR 211.52

Regulatory notes

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

Interactions

429 interactions on record for adalimumab.

Graded by severity as the source publishes them — 286 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

Adalimumab · interactions on record

429 records

  • 286 severe
  • 136 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

Adalimumab in 15 other countries

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

All adalimumab products

Authorised across Europe · EMA

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

  • United Kingdom (Northern Ireland) · Hukyndra, Humira
  • Iceland · Amgevita, Amsparity
  • Liechtenstein · Amsparity, Hefiya
  • Norway · Amgevita, Amsparity

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 Base de données publique des médicaments — BDPM (France). 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/a9391ec8-d022-453e-a4d4-41125e5b429a
GET /v1/drugs/a9391ec8-d022-453e-a4d4-41125e5b429a?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.

{
  "cis": "62975984",
  "date_amm": "2017-12-08",
  "type_amm": "Procédure centralisée",
  "numero_ue": "EU/1/03/256",
  "substance": "ADALIMUMAB",
  "atc_source": "fr_atc_restore_2026-09-06",
  "statut_amm": "Autorisation active",
  "statut_bdm": null,
  "forme_pharmaceutique": "solution injectable",
  "voies_administration": "sous-cutanée",
  "etat_commercialisation": "Commercialisée",
  "surveillance_renforcee": "Non"
}

See everything about adalimumab.

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.