Poland· PL-100437188

Condyline

A podophyllotoxin product containing podophyllotoxinum, registered in Poland by Medezin Sp. z o.o.. 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-100437188PACKS LISTED1CHECKEDSeptember 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
Medezin Sp. z o.o.
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 · 1

  • gtin
    05909991432225

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/7be31e59-63d3-4bb6-9156-59ea9613f075
GET /v1/drugs/7be31e59-63d3-4bb6-9156-59ea9613f075?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": "05909991432225 ¦ Rp ¦ 136701\n1 butelka 3,5 ml",
  "substance": null,
  "common_name": "Podophyllotoxinum",
  "pl_product_id": "100437188",
  "pozwolenie_nr": "177/20",
  "auth_procedure": "IR",
  "authorisation_validity": "2030-07-09"
}

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.