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Belgium· BE-AMP-SAM465573-00

Zydelig 100 mg

A idelalisib product containing idelalisib, registered in Belgium by Gilead Sciences Ireland UC. The same ATC class is registered in 12 of our 19 countries.

ATC L01EM01

Checked against FAMHP / AFMPS (Belgium) on

Informational only — not a medical device.

SOURCE REGISTER · BEFAMHP / AFMPS (Belgium)normalisedZydelig 100 mgATCL01EM01REGISTER NO.BE-AMP-SAM465573-00PACKS LISTED2CHECKEDSeptember 26, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about idelalisibAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Idelalisib is registered in 12 of 19 countries.

Countries holding a registration under ATC L01EM01 (idelalisib), each read from that country’s own register.

  • This record: Belgium, from FAMHP / AFMPS (Belgium)
  • 8 of them publish a price we can compare per daily dose
Search idelalisib products by name

Idelalisib · ATC L01EM01

12 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • 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 idelalisib costs, country by country.

Normalised to the WHO defined daily dose (0.3 g), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown
Open the full comparison — free accountDrug prices for market access

Idelalisib · price per daily dose (0.3 g)

USD · FX 28 Sept 2026

  • CH Switzerland$222.92
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

FAMHP / AFMPS (Belgium)
Active substance
Idelalisib
Manufacturer
Gilead Sciences Ireland UC
Country
Belgium (BE)
ATC code
L01EM01
ATC class
Idelalisib
Defined daily dose
0.3 g, O
Reimbursed
Not published by this register
Source register
FAMHP / AFMPS (Belgium)
Last checked
September 26, 2026

Packs & prices · 2

  • be_apb
    7714207
  • be_apb
    3303906

Regulatory notes

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

Interactions

820 interactions on record for idelalisib.

Graded by severity as the source publishes them — 236 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 idelalisib against other medicinesHow interaction checks work

Idelalisib · interactions on record

820 records

  • 236 severe
  • 568 moderate
  • 16 minor

Most severe, free to view

  • CisaprideA03FA02severe
  • NaloxegolA06AH03severe
  • LoperamideA07DA03severe
  • BudesonideA07EA06severe
  • 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

Idelalisib in 13 other countries

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

All idelalisib products

Authorised across Europe · EMA

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

  • Iceland · Zydelig
  • Liechtenstein · Zydelig
  • Norway · Zydelig

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/fb203b07-9e27-435a-889f-e1d99d20d5c3
GET /v1/drugs/fb203b07-9e27-435a-889f-e1d99d20d5c3?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": "Film-coated tablet",
  "source": "afmps",
  "status": "AUTHORIZED",
  "name_en": "Zydelig 100 mg",
  "name_fr": "Zydelig 100 mg",
  "name_nl": "Zydelig 100 mg",
  "amp_code": "SAM465573-00",
  "strengths": [
    "100.0000",
    "0.1000"
  ],
  "pack_count": 1,
  "substances": [
    "Idelalisib",
    "E 110",
    "Sodium Starch Glycolate (Type A)"
  ],
  "medicine_type": "ALLOPATHIC",
  "atc_description": "Idelalisib",
  "authorisation_numbers": [
    "EU/1/14/938/001"
  ]
}
API referenceMCP serverPlans

See everything about idelalisib.

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.

Try it freeOpen in the console