Poland· PL-100006092
Antithrombin III NF Takeda
A antithrombin iii product containing antithrombinum iii humanum densatum, registered in Poland by Takeda Pharma Sp. z o.o.. The same ATC class is registered in 11 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Antithrombin iii is registered in 11 of 19 countries.
Countries holding a registration under ATC B01AB02 (antithrombin iii), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 6 of them publish a price we can compare per daily dose
Antithrombin iii · ATC B01AB02
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Germany
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
The record
At a glance
URPL (Poland)- Active substance
- Antithrombinum III humanum densatum
- Manufacturer
- Takeda Pharma Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- B01AB02
- ATC class
- Antithrombin III
- Defined daily dose
- 2.1 TSD, E
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin05909990302413
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
112 interactions on record for antithrombin iii.
Graded by severity as the source publishes them — 41 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
Antithrombin iii · interactions on record
112 records
- 41 severe
- 71 moderate
Most severe, free to view
- DalteparinB01AB04severe
- EnoxaparinB01AB05severe
- DanaparoidB01AB09severe
- TinzaparinB01AB10severe
- 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
Antithrombin iii in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaANBINEXInstituto Grifols, S.A., Barcelona
- SpainANBINEX POLVO Y DISOLVENTE PARA SOLUCION PARA PERFUSIONInstituto Grifols S.A.
- NorwayAtenativOrifarm AS
- SwitzerlandAtenativ 1000 I.E., Pulver und Lösungsmittel zur Herstellung einer InfusionslösungOctapharma AG
- BelgiumAtenativ 1000 IUOctapharma Benelux
- SwedenAntithrombin III Baxalta Pulver och vätska till injektions-/infusionsvätska, lösningBaxalta Innovations GmbH
- GermanyAnbinexGrifols Deutschland Gmbh
- United KingdomAntithrombin III 1,000unit powder and solvent for solution for infusion vialsImported (Austria)
Authorised across Europe · EMA
The same active substance is authorised in 25 EEA countries. Names it is sold under:
- Austria · Antithrombin Iii Takeda, Atenativ
- Belgium · Antithrombin Iii Konzentrat Baxalta, Antitrombine Iii-Concentraat Baxalta
- Bulgaria · Антитромбин Iii Nf Получен От Човешка Плазма Баксалта, Атенатив
- Czechia · Anbinex, Antithrombin Iii Baxalta
- Germany · Anbinex, Atenativ
- Denmark · Antitrombin Iii Baxalta, Atenativ
- Estonia · Atenativ
- Spain · Anbinex, Kybernin P
- Finland · Atenativ
- France · Aclotine, Atenativ
- Greece · Kybernin P
- Croatia · Antithrombin Iii Baxalta, Atenativ
- Hungary · Antithrombin Iii Baxalta, Atenativ
- Italy · Anbinex, Anternaty
- Lithuania · Atenativ
- Luxembourg · Kybernin P
- Latvia · Atenativ
- Malta · Antithrombin Iii Baxalta
- Netherlands · Antitrombine Iii Concentraat Baxalta, Atenativ
- Norway · Atenativ
- Portugal · Anbinex, Atenativ
- Romania · Atenativ
- Sweden · Antithrombin Iii Baxalta, Antithrombin Iii Octapharma
- Slovenia · Atenativ, Kybernin P
- Slovakia · Anbinex, Antithrombin Iii Ľudský Antitrombín Iii Získaný Z Plazmy Baxalta
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/c133a165-e6bf-4604-b6e9-4cac4be5547f GET /v1/drugs/c133a165-e6bf-4604-b6e9-4cac4be5547f?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 i rozpuszczalnik do sporządzania roztworu do infuzji",
"source": "urpl",
"strength": "50 j.m./ml; 500 j.m.",
"packaging": "05909990302413 ¦ Lz ¦ 20818\n1 fiol. proszku ¦ 1 fiol. 10 ml rozp. ¦ 1 zestaw do sporządzania i podania roztworu",
"substance": "Antithrombinum humanum III 50 j.m./ml; 500 j.m.",
"common_name": "Antithrombinum III humanum densatum",
"pl_product_id": "100006092",
"pozwolenie_nr": "03024",
"auth_procedure": "NAR",
"authorisation_validity": "Bezterminowe"
}See everything about antithrombin iii.
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.