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.
Checked against URPL (Poland) on
Informational only — not a medical device.
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
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
- gtin05901797710989
- gtin05901797710972
- gtin05397315000067
- gtin05397315000074
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.
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.
- CzechiaABEVMYBiosimilar Collaborations Ireland Limited, Dublin
- BelgiumAbevmy 25 mg/mlBiosimilar Collaborations Ireland
- FinlandAbevmyBiosimilar Collaborations Ireland Limited
- IrelandAbevmy 25 mg/mL concentrate for solution for infusionBiosimilar Collaborations Ireland Limited
- IcelandAbevmyBiosimilar Collaborations Ireland Limited
- SwedenAbevmy 25 mg/ml Koncentrat till infusionsvätska, lösningBiosimilar Collaborations Ireland Limited
- NorwayAlymsysMabxience Research SL
- United KingdomAbevmy 100mg/4ml concentrate for solution for infusion vialsBiocon Biologics Ireland Ltd
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.