Netherlands· NL-e1e7225247a4
Dovprela 200 mg tablet
A pretomanid product containing pretomanid, registered in Netherlands by Mylan IRE Healthcare Limited. The same ATC class is registered in 10 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Pretomanid is registered in 10 of 19 countries.
Countries holding a registration under ATC J04AK08 (pretomanid), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 7 of them publish a price we can compare per daily dose
Pretomanid · ATC J04AK08
10 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Netherlands
- Norwayprice
- Polandprice
- United Kingdom
- United Statesprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- PRETOMANID
- Manufacturer
- Mylan IRE Healthcare Limited
- Country
- Netherlands (NL)
- ATC code
- J04AK08
- ATC class
- Pretomanid
- Defined daily dose
- 0.2 g, O
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_idEU/1/20/1437
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
20 interactions on record for pretomanid.
Graded by severity as the source publishes them — 9 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
Pretomanid · interactions on record
20 records
- 9 severe
- 11 moderate
Most severe, free to view
- DexamethasoneH02AB02severe
- DabrafenibL01EC02severe
- LorlatinibL01ED05severe
- DabrafenibL01XE23severe
- 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
Pretomanid in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaDOVPRELAMylan IRE Healthcare Limited, Dublin
- FinlandDovprelaMylan IRE Healthcare Limited
- FranceDOVPRELA 200 mg, compriméMYLAN IRE HEALTHCARE (IRLANDE)
- United KingdomDovprela 200mg tabletsImported (Italy)
- IrelandDovprela 200 mg tabletsMylan IRE Healthcare Limited
- IcelandDovprelaMylan IRE Healthcare Limited
- NorwayDovprelaMylan
- PolandDovprelaMylan IRE Healthcare Ltd.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Dovprela
- Liechtenstein · Dovprela
- Norway · Dovprela
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 CBG-MEB (Netherlands). 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/59afc9df-b3ca-49df-8ddc-96d1d6b5a2e3 GET /v1/drugs/59afc9df-b3ca-49df-8ddc-96d1d6b5a2e3?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": "Tablet",
"route": "Oraal gebruik",
"soort": null,
"source": "cbg_meb",
"smpc_url": "https://www.ema.europa.eu/en/documents/product-information/dovprela-epar-product-information_nl.pdf",
"strength": null,
"atc_label": "Pretomanid",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/cp124660",
"excipients": [
"CELLULOSE, MICROKRISTALLIJN (E 460(i))",
"LACTOSE 1-WATER",
"MAGNESIUMSTEARAAT (E 470b)",
"NATRIUMLAURILSULFAAT",
"NATRIUMZETMEELGLYCOLAAT",
"POVIDON K 30 (E 1201)",
"SILICIUMDIOXIDE (E 551)"
],
"substances": [
"PRETOMANID"
],
"leaflet_url": null,
"authorised_at": "2020/07/31",
"procedure_number": "EMEA/H/C/005167",
"dispensing_status": "Uitsluitend recept",
"registration_number": "EU/1/20/1437",
"additional_monitoring": "Y"
}See everything about pretomanid.
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.