Poland· PL-100449085

Abevmy

A bevacizumab product containing bevacizumabum, registered in Poland by Biosimilar Collaborations Ireland Ltd. The same ATC class is registered in 3 of our 19 countries.

ATC L01XC07

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedAbevmyATCL01XC07REGISTER NO.PL-100449085PACKS LISTED4CHECKEDSeptember 27, 2026

Where it is registered

Bevacizumab is registered in 3 of 19 countries.

Countries holding a registration under ATC L01XC07 (bevacizumab), 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

Bevacizumab · ATC L01XC07

3 / 19 countries

  • Belgiumprice
  • Ireland
  • 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
Bevacizumabum
Manufacturer
Biosimilar Collaborations Ireland Ltd
Country
Poland (PL)
ATC code
L01XC07
ATC class
Bevacizumab
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 4

  • gtin
    05901797710989
  • gtin
    05901797710972
  • gtin
    05397315000067
  • gtin
    05397315000074

Regulatory notes

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

Interactions

22 interactions on record for bevacizumab.

Graded by severity as the source publishes them — 6 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

Bevacizumab · interactions on record

22 records

  • 6 severe
  • 16 moderate

Most severe, free to view

  • SunitinibL01EX01severe
  • PanitumumabL01FE02severe
  • PanitumumabL01XC08severe
  • SunitinibL01XE04severe
  • 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

Bevacizumab in 15 other countries

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

All bevacizumab products

Authorised across Europe · EMA

The same active substance is authorised in 4 EEA countries. Names it is sold under:

  • United Kingdom (Northern Ireland) · Oyavas
  • Iceland · Abevmy, Alymsys
  • Liechtenstein · Abevmy, Alymsys
  • Norway · Abevmy, Alymsys

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/0e02bc5b-ba52-4e1a-bc78-26ff7a5d1ce3
GET /v1/drugs/0e02bc5b-ba52-4e1a-bc78-26ff7a5d1ce3?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": "Koncentrat do sporządzania roztworu do infuzji",
  "source": "urpl",
  "strength": "25 mg/ml",
  "packaging": "05901797710989 ¦ Rpz ¦ EU/1/20/1515/003 ¦ 139570\n1 fiol. 16 ml\n05901797710972 ¦ Rpz ¦ EU/1/20/1515/001 ¦ 139571\n1 fiol. 4 ml\nRpz ¦ EU/1/20/1515/004 ¦ 139572\n2 fiol. 16 ml\nRpz ¦ EU/1/20/1515/005 ¦ 139573\n3 fiol. 16 ml\nRpz ¦ EU/1/20/1515/002 ¦ 139574\n5 fiol. 4 ml\n05397315000067 ¦ Rpz ¦ EU/1/20/1515/001 ¦ 158818\n1 fiol. 4 ml\n05397315000074 ¦ Rpz ¦ EU/1/20/1515/003 ¦ 158819\n1 fiol. 16 ml",
  "substance": "Bevacizumabum 25 mg/ml",
  "common_name": "Bevacizumabum",
  "pl_product_id": "100449085",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about bevacizumab.

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.