Switzerland· 70087001

Flixabi

A infliximab product containing infliximabum, registered in Switzerland and dispensed under Swissmedic category A, on the national reimbursement list. The same ATC class is registered in 14 of our 19 countries.

Reimbursed in Switzerland (BAG SL)Cat A (Swissmedic)ATC L04AB02

Checked against BAG Spezialitätenliste (Switzerland) on

Informational only — not a medical device.

SOURCE REGISTER · CHBAG Spezialitätenliste (Switzerland)normalisedFlixabiATCL04AB02REGISTER NO.70087001PACKS LISTED1CHECKEDSeptember 12, 2026

Where it is registered

Infliximab is registered in 14 of 19 countries.

Countries holding a registration under ATC L04AB02 (infliximab), each read from that country’s own register.

  • This record: Switzerland, from BAG Spezialitätenliste (Switzerland)
  • 9 of them publish a price we can compare per daily dose

Infliximab · ATC L04AB02

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 infliximab costs, country by country.

Normalised to the WHO defined daily dose (3.75 mg), the median price runs from $0.31 in Finland to $24.45 in Switzerland — a ×79 gap.

  • Switzerland: $24.45 per daily dose (median across products in the class)
  • Public list prices, converted to USD at the rate date shown

Infliximab · price per daily dose (3.75 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$24.45
  • FI Finland$0.31
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

BAG Spezialitätenliste (Switzerland)
Active substance
infliximabum
Manufacturer
—
Country
Switzerland (CH)
ATC code
L04AB02
ATC class
Infliximab
Defined daily dose
3.75 mg, P
Swissmedic category
A
Reimbursed
Yes
Source register
BAG Spezialitätenliste (Switzerland)
Last checked
September 12, 2026

Packs & prices · 1

1 priced
  • gtin
    7680700870016
    1 Stk
    CHF 554.75

Regulatory notes

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

Interactions

443 interactions on record for infliximab.

Graded by severity as the source publishes them — 290 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

Infliximab · interactions on record

443 records

  • 290 severe
  • 146 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

Infliximab in 16 other countries

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

All infliximab products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Remicade, Remsima
  • Liechtenstein · Remicade, Remsima
  • Norway · Remicade, Remsima

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 BAG Spezialitätenliste (Switzerland). 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/ea064836-4c89-475c-8e01-cbdeb99c8ba4
GET /v1/drugs/ea064836-4c89-475c-8e01-cbdeb99c8ba4?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.

{
  "unit": null,
  "strength": "infliximabum",
  "valid_from": "2026-08-01",
  "limitations": "[{\"description\":\"<p><strong>Austausch Referenzpr&auml;parat/Biosimilar</strong><br>Die Behandlung mit FLIXABI bedarf der Kostengutsprache durch den Krankenversicherer nach vorg&auml;ngiger Konsultation des Vertrauensarztes. F&uuml;r die Behandlung mit FLIXABI ist keine neue Kostengutsprache n&ouml;tig, wenn in derselben Indikation bereits eine Kostengutsprache f&uuml;r das Referenzpr&auml;parat oder ein anderes Biosimilar besteht.</p>\",\"costApproval\":null,\"indication\":\"22067.XX\",\"isNew\":true,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2026-08-01\",\"validTo\":null},{\"description\":\"<p><strong>Aktive Rheumatoide Arthritis</strong><br>Behandlung der aktiven rheumatoiden Arthritis, wenn die vorausgegangene antirheumatische Standardtherapie mit krankheitsmodifizierenden Antirheumatika (DMARDs) unzul&auml;nglich war.</p>\",\"costApproval\":null,\"indication\":\"22067.01\",\"isNew\":true,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2026-08-01\",\"validTo\":null},{\"description\":\"<p><strong>Morbus Crohn</strong><br>Behandlung von Patienten mit aktivem Morbus Crohn, wenn die vorausgegangene konventionelle Therapie (z.B. mit Azathioprin, 6-Mercaptopurin, Steroiden) unzul&auml;nglich war.</p>\",\"costApproval\":null,\"indication\":\"22067.02\",\"isNew\":true,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2026-08-01\",\"validTo\":null},{\"description\":\"<p><strong>Morbus Bechterew/Ankylosierende Spondylitis</strong><br>Behandlung des Morbus Bechterew, wenn die vorausgegangene konventionelle Therapie unzul&auml;nglich war.</p>\",\"costApproval\":null,\"indication\":\"22067.03\",\"isNew\":true,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2026-08-01\",\"validTo\":null},{\"description\":\"<p><strong>Moderate bis schwere Colitis ulcerosa</strong><br>Behandlung erwachsener Patienten mit INFLIXIMAB, wenn die vorausgegangene konventionelle Therapie (z.B. mit Azathioprin, 6-Mercaptopurin oder Glukokortikoiden) unzul&auml;nglich war oder nicht vertragen wurde.<br><br>Die Verschreibung von INFLIXIMAB f&uuml;r die folgenden Behandlungen kann nur durch Fach&auml;rzte der Rheumatologie/Dermatologie oder rheumatologische/dermatologische Universit&auml;tskliniken/Polikliniken erfolgen:</p>\",\"costApproval\":null,\"indication\":\"22067.04\",\"isNew\":true,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2026-08-01\",\"validTo\":null},{\"description\":\"<p><strong>Schwere Plaque-Psoriasis</strong><br>Behandlung erwachsener Patienten mit schwerer Plaque-Psoriasis, bei denen 1.) eine Phototherapie oder eine der folgenden konventionellen systemischen Therapien (Ciclosporin, Methotrexat, Acitretin) keinen therapeutischen Erfolg gezeigt haben, und 2.) eine TNF-alpha blockierende Substanz (z.B. Etanercept) keinen therapeutischen Erfolg gezeigt hat. Falls nach 14 Wochen kein therapeutischer Erfolg eingetreten ist, ist die Behandlung abzubrechen. Die maximale Behandlungsdauer betr&auml;gt 1 Jahr.</p>\",\"costApproval\":null,\"indication\":\"22067.05\",\"isNew\":true,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2026-08-01\",\"validTo\":null},{\"description\":\"<p><strong>Psoriasis Arthritis</strong><br>Behandlung erwachsener Patienten mit aktiver Psoriasis-Arthritis 1.) nur in Kombination mit Methotrexat, bei Versagen von mindestens zwei krankheitsmodifizierenden DMARD inklusive Methotrexat und 2.) nach Versagen der Kombinationen Methotrexat/Etanercept oder Methotrexat/Adalimumab.</p>\",\"costApproval\":null,\"indication\":\"22067.06\",\"isNew\":true,\"limitationCode\":null,\"points\":null,\"priceModel\":null,\"title\":null,\"validFrom\":\"2026-08-01\",\"validTo\":null}]",
  "galenic_form": "Trockensub 100 mg Durchstf",
  "therapeutic_area": null,
  "sl_inclusion_date": "2026-08-01",
  "self_retention_pct": 10
}

See everything about infliximab.

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.