Poland· PL-100459990

Ronapreve

A casirivimab and imdevimab product containing casirivimabum + imdevimabum, registered in Poland by Roche Registration GmbH. The same ATC class is registered in 5 of our 19 countries.

ATC J06BD07

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedRonapreveATCJ06BD07REGISTER NO.PL-100459990PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Casirivimab and imdevimab is registered in 5 of 19 countries.

Countries holding a registration under ATC J06BD07 (casirivimab and imdevimab), each read from that country’s own register.

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

Casirivimab and imdevimab · ATC J06BD07

5 / 19 countries

  • Belgiumprice
  • Denmark
  • Finlandprice
  • Polandprice
  • Spainprice
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
Casirivimabum + Imdevimabum
Manufacturer
Roche Registration GmbH
Country
Poland (PL)
ATC code
J06BD07
ATC class
Casirivimab and imdevimab
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    07613326052658
  • gtin
    07613326052740

Regulatory notes

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

Same medicine, other countries

Casirivimab and imdevimab in 2 other countries

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

All casirivimab and imdevimab products

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/10b53b5c-6953-4b1a-bd16-80829fa2e327
GET /v1/drugs/10b53b5c-6953-4b1a-bd16-80829fa2e327?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": "Roztwór do wstrzykiwań i infuzji",
  "source": "urpl",
  "strength": "120 mg/ml + 120 mg/ml",
  "packaging": "07613326052658 ¦ Rp ¦ EU/1/21/1601/002 ¦ 142399\n1 fiol. 11,1 ml roztworu kazyrywymabu ¦ 1 fiol. 11,1 ml roztworu imdewymabu\n07613326052740 ¦ Rp ¦ EU/1/21/1601/001 ¦ 142482\n1 fiol. 2,5 ml roztworu kazyrywymabu ¦ 1 fiol. 2,5 ml roztworu imdewymabu",
  "substance": "Casirivimabum 120 mg/ml + Imdevimabum 120 mg/ml",
  "common_name": "Casirivimabum + Imdevimabum",
  "pl_product_id": "100459990",
  "pozwolenie_nr": null,
  "auth_procedure": "CEN",
  "authorisation_validity": null
}

See everything about casirivimab and imdevimab.

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.