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Ireland· IE-PA-PA22643/002/003

Monotrim 200 mg Tablets

A trimethoprim product containing trimethoprim, registered in Ireland by Chemidex Pharma Limited. The same ATC class is registered in 12 of our 19 countries.

ATC J01EA01

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedMonotrim 200 mg TabletsATCJ01EA01REGISTER NO.IE-PA-PA22643/002/003PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Trimethoprim is registered in 12 of 19 countries.

Countries holding a registration under ATC J01EA01 (trimethoprim), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 6 of them publish a price we can compare per daily dose

Trimethoprim · ATC J01EA01

12 / 19 countries

  • Canada
  • Denmark
  • Finlandprice
  • Franceprice
  • Germany
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • United Kingdom
  • United Statesprice
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.

Price per daily dose

What a daily dose of trimethoprim costs, country by country.

Normalised to the WHO defined daily dose (0.4 g), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown

Trimethoprim · price per daily dose (0.4 g)

USD · FX 28 Sept 2026

  • FR France$2.50
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

HPRA (Ireland)
Active substance
Trimethoprim
Manufacturer
Chemidex Pharma Limited
Country
Ireland (IE)
ATC code
J01EA01
ATC class
Trimethoprim
Defined daily dose
0.4 g, O
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    PA22643/002/003

Regulatory notes

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

Interactions

138 interactions on record for trimethoprim.

Graded by severity as the source publishes them — 12 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

Trimethoprim · interactions on record

138 records

  • 12 severe
  • 33 moderate
  • 2 minor
  • 91 info

Most severe, free to view

  • Potassium chlorideA12BA01severe
  • Potassium citrateA12BA02severe
  • Potassium gluconateA12BA05severe
  • Potassium chlorideB05XA01severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Trimethoprim in 13 other countries

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

All trimethoprim products

Authorised across Europe · EMA

The same active substance is authorised in 15 EEA countries. Names it is sold under:

  • Austria · Motrim, Triprim
  • Germany · Infectotrimet
  • Denmark · Trimopan
  • Estonia · Trimetop
  • Spain · Tediprima
  • Finland · Trimetin, Trimopan
  • France · Delprim
  • United Kingdom (Northern Ireland) · Trimethoprim, Trimethoprim Accord-Uk
  • Iceland · Idotrim, Trimetoprim Viatris
  • Lithuania · Trimetop
  • Latvia · Trimetop
  • Netherlands · Trimethoprim Cf, Trimethoprim Mylan
  • Norway · Trimetoprim Orion
  • Poland · Trimesan, Urotrim
  • Sweden · Idotrim, Trimetoprim Viatris

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 HPRA (Ireland). 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/dcc87bfc-4ab1-44f8-961a-41d090351332
GET /v1/drugs/dcc87bfc-4ab1-44f8-961a-41d090351332?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",
  "routes": [
    "Oral use"
  ],
  "source": "hpra",
  "atc_all": [
    "J01EA",
    "J01EA01"
  ],
  "strength": null,
  "pa_number": "PA22643/002/003",
  "substances": [
    "Trimethoprim"
  ],
  "legal_basis": "Generic application (Article 10(1) of Directive No 2001/83/EC)",
  "market_info": "Marketed",
  "authorised_at": "19/06/2009",
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": "IC0187-067-002"
}

See everything about trimethoprim.

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.