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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.

ATC B01AB02

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedAntithrombin III NF TakedaATCB01AB02REGISTER NO.PL-100006092PACKS LISTED1CHECKEDSeptember 27, 2026

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
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.

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

  • gtin
    05909990302413

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.
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

Antithrombin iii in 13 other countries

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

All antithrombin iii products

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.