Poland· PL-100015620

Condyline

A podophyllotoxin product containing podophyllotoxinum, registered in Poland by Karo Pharma AB. The same ATC class is registered in 9 of our 19 countries.

ATC D06BB04

Checked against URPL (Poland) on

Informational only — not a medical device.

SOURCE REGISTER · PLURPL (Poland)normalisedCondylineATCD06BB04REGISTER NO.PL-100015620PACKS LISTED2CHECKEDSeptember 27, 2026

Where it is registered

Podophyllotoxin is registered in 9 of 19 countries.

Countries holding a registration under ATC D06BB04 (podophyllotoxin), 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

Podophyllotoxin · ATC D06BB04

9 / 19 countries

  • Denmark
  • Finlandprice
  • Franceprice
  • Germany
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • 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
Podophyllotoxinum
Manufacturer
Karo Pharma AB
Country
Poland (PL)
ATC code
D06BB04
ATC class
Podophyllotoxin
Reimbursed
Not published by this register
Source register
URPL (Poland)
Last checked
September 27, 2026

Packs & prices · 2

  • gtin
    05909990299515
  • gtin
    07350087730318

Regulatory notes

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

Same medicine, other countries

Podophyllotoxin in 10 other countries

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

All podophyllotoxin products

Authorised across Europe · EMA

The same active substance is authorised in 9 EEA countries. Names it is sold under:

  • Germany · Wartec
  • Spain · Wartec
  • France · Condyline
  • United Kingdom (Northern Ireland) · Podophyllotoxin Phoenix Labs, Warticon
  • Ireland · Warticon
  • Italy · Condyline
  • Netherlands · Condyline, Wartec
  • Romania · Condyline
  • Sweden · Wartec

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/20a05de4-cc96-43cb-940d-ca22af6ae348
GET /v1/drugs/20a05de4-cc96-43cb-940d-ca22af6ae348?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 na skórę",
  "source": "urpl",
  "strength": "5 mg/ml",
  "packaging": "05909990299515 ¦ Rp ¦ Skasowane ¦ 2680\n1 butelka 3,5 ml\n07350087730318 ¦ Rp ¦ 139828\n1 butelka 3,5 ml",
  "substance": "Podophyllotoxinum 5 mg/ml",
  "common_name": "Podophyllotoxinum",
  "pl_product_id": "100015620",
  "pozwolenie_nr": "02995",
  "auth_procedure": "NAR",
  "authorisation_validity": "Bezterminowe"
}

See everything about podophyllotoxin.

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.