Poland· PL-100512748
Desferal
A deferoxamine product containing deferoxamini mesilas, registered in Poland by Delfarma Sp. z o.o.. The same ATC class is registered in 16 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Deferoxamine is registered in 16 of 19 countries.
Countries holding a registration under ATC V03AC01 (deferoxamine), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 10 of them publish a price we can compare per daily dose
Deferoxamine · ATC V03AC01
16 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Italyprice
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Statesprice
Price per daily dose
What a daily dose of deferoxamine costs, country by country.
Normalised to the WHO defined daily dose (2.8 g), so markets compare like for like.
- 2 markets with a comparable price for this class
- Public list prices, converted to USD at the rate date shown
Deferoxamine · price per daily dose (2.8 g)
USD · FX 28 Sept 2026
- CH Switzerland$48.38
- FR France$33.66
The record
At a glance
URPL (Poland)- Active substance
- Deferoxamini mesilas
- Manufacturer
- Delfarma Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- V03AC01
- ATC class
- Deferoxamine
- Defined daily dose
- 2.8 g, P
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin05909991564384
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
49 interactions on record for deferoxamine.
Graded by severity as the source publishes them — 9 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
Deferoxamine · interactions on record
49 records
- 9 severe
- 5 moderate
- 35 info
Most severe, free to view
- CidofovirJ05AB12severe
- VigabatrinN03AG04severe
- InotersenN07XX15severe
- IopamidolV08AB04severe
- 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.
Same medicine, other countries
Deferoxamine in 15 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomDesferal 500mg powder for solution for injection vialsWaymade Healthcare Plc
- BelgiumDesferal 500 mgMitem Pharma
- United StatesDeferoxamineFresenius Kabi USA, LLC
- GermanyDeferoxaminmesilat Noridem EnterprisesNoridem Enterprises Ltd
- ItalyDEFEROXAMINA NORIDEMNORIDEM ENTERPRISES LTD
- CanadaDEFEROXAMINE MESYLATE FOR INJECTIONPFIZER CANADA ULC
- NorwayDesferal2care4 ApS
- SwedenDesferal 500 mg Pulver till injektions-/infusionsvätska, lösningMITEM PHARMA
Authorised across Europe · EMA
The same active substance is authorised in 22 EEA countries. Names it is sold under:
- Austria · Desferal
- Belgium · Desferal
- Bulgaria · Десферал
- Cyprus · Deferoxamine Noridem
- Czechia · Desferal
- Germany · Deferoxaminmesilat Noridem Enterprises, Desferal
- Denmark · Desferal
- Spain · Desferin
- Finland · Desferal
- France · Desferal
- United Kingdom (Northern Ireland) · Desferrioxamine Mesilate Noridem Enterprises
- Greece · Deferoxamine Noridem, Demoferidon
- Hungary · Desferal
- Ireland · Desferal
- Iceland · Desferal
- Italy · Deferoxamina Noridem, Desferal
- Luxembourg · Desferal
- Netherlands · Desferal
- Norway · Desferal
- Portugal · Desferal
- Romania · Desferal
- Sweden · Desferal
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 URPL (Poland). 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/cbd0f3d2-5500-4521-9e02-dd8a4c7d187e GET /v1/drugs/cbd0f3d2-5500-4521-9e02-dd8a4c7d187e?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": "Proszek do sporządzania roztworu do wstrzykiwań",
"source": "urpl",
"strength": "500 mg",
"packaging": "05909991564384 ¦ Rp ¦ 160312\n10 fiol. 500 mg w proszku",
"substance": "Deferoxamini mesilas 500 mg",
"common_name": "Deferoxamini mesilas",
"pl_product_id": "100512748",
"pozwolenie_nr": "041/25",
"auth_procedure": "IR",
"authorisation_validity": "2030-01-29"
}See everything about deferoxamine.
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.