Poland· PL-100380637

Sulovas

A sulodexid product containing sulodexidum, registered in Poland by Aflofarm Farmacja Polska Sp. z o.o.. The same ATC class is registered in 2 of our 19 countries.

ATC B01AB11

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedSulovasATCB01AB11REGISTER NO.PL-100380637PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Sulodexid is registered in 2 of 19 countries.

Countries holding a registration under ATC B01AB11 (sulodexid), each read from that country’s own register.

  • This record: Poland, from URPL (Poland)
  • 2 of them publish a price we can compare per daily dose

Sulodexid · ATC B01AB11

2 / 19 countries

  • Czechiaprice
  • Polandprice
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
Sulodexidum
Manufacturer
Aflofarm Farmacja Polska Sp. z o.o.
Country
Poland (PL)
ATC code
B01AB11
ATC class
Sulodexid
Defined daily dose
500 LSU, O
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05909991384159
  • gtin
    05902802709707

Regulatory notes

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

Same medicine, other countries

Sulodexid in 2 other countries

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

All sulodexid products

Authorised across Europe · EMA

The same active substance is authorised in 8 EEA countries. Names it is sold under:

  • Bulgaria · Трепарин
  • Czechia · Vessel Due F
  • Spain · Aterina, Dovida
  • Hungary · Vessel Due, Vessel Due F
  • Italy · Angioflux, Provenal
  • Portugal · Treparin, Vessel
  • Romania · Coreflux, Vessel Due F
  • Slovakia · Vessel Due F

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/439b40b1-1e66-4693-8200-6e96e8fdddba
GET /v1/drugs/439b40b1-1e66-4693-8200-6e96e8fdddba?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": "Kapsułki miękkie",
  "source": "urpl",
  "strength": "250 LSU",
  "packaging": "05909991384159 ¦ Rp ¦ 128875\n50 kaps.\n05902802709707 ¦ Rp ¦ 164921\n10 kaps.",
  "substance": "Sulodexidum 250 LSU (25 mg)",
  "common_name": "Sulodexidum",
  "pl_product_id": "100380637",
  "pozwolenie_nr": "24968",
  "auth_procedure": "NAR",
  "authorisation_validity": "Bezterminowe"
}

See everything about sulodexid.

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.