Ireland· IE-PA-PA1335/002/001

Cefixime 200 mg film-coated tablets

A other beta-lactam antibacterials product containing cefixime trihydrate, registered in Ireland by Orchid Europe Limited.

ATC J01D

Checked against HPRA (Ireland) on September 28, 2026

Informational only — not a medical device.

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The record

At a glance

HPRA (Ireland)

Active substance: CEFIXIME TRIHYDRATE
Manufacturer: Orchid Europe Limited
Country: Ireland (IE)
ATC code: J01D
ATC class: OTHER BETA-LACTAM ANTIBACTERIALS
Reimbursed: Not published by this register
Source register: HPRA (Ireland)
Last checked: September 28, 2026

Packs & prices · 1

ie_pa_number
PA1335/002/001

Regulatory notes

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

Same medicine, other countries

Cefixime trihydrate in 12 other countries

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

All cefixime trihydrate products

Authorised across Europe · EMA

The same active substance is authorised in 21 EEA countries. Names it is sold under:

Austria · Cefixim Nectar, Sorcelif
Bulgaria · Cefixime Neclife, Cefixime Viatris
Cyprus · Cefimed, Cefixime Viatris
Czechia · Cefixime Innfarm, Sorcelif
Germany · Cefixim Al, Cefixim Aristo
Spain · Afixora, Cefixima Neclife
France · Cefixime Almus, Cefixime Arrow
United Kingdom (Northern Ireland) · Suprax
Greece · Ceftoral
Croatia · Cefiksim Alkaloid, Cefiksim Nectar
Hungary · Cefixim Nectar, Cefixime Reiwa Healthcare
Italy · Cefixima Aurobindo, Cefixima Doc Generici
Lithuania · Cefixime Medochemie
Malta · Tricef
Norway · Cefixime Frostpharma, Cefixime Medochemie
Poland · Cetix, Xifia
Portugal · Cefiton, Cefixim Nectar
Romania · Axtrifia, Cefiximă Medochemie
Sweden · Cefixime Frostpharma, Cefixime Medochemie
Slovenia · Pancef
Slovakia · Cefimed, Cefixim

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/c37032a9-66b4-4081-bf93-4f6897dee21d
GET /v1/drugs/c37032a9-66b4-4081-bf93-4f6897dee21d?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": "Film-coated tablet",
  "routes": [
    "Oral use"
  ],
  "source": "hpra",
  "atc_all": [
    "J01D"
  ],
  "strength": null,
  "pa_number": "PA1335/002/001",
  "substances": [
    "CEFIXIME TRIHYDRATE"
  ],
  "legal_basis": "Generic application (Article 10(1) of Directive No 2001/83/EC)",
  "market_info": "Not marketed",
  "authorised_at": "15/10/2010",
  "dispensing_status": "Product subject to prescription which may not be renewed (A)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

API reference MCP server Plans

See everything about cefixime trihydrate.

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.

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