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Ireland· IE-PA-PA1113/007/001

Casacol Expectorant SyrupMethoxyphenamine hydrochloride 20 mg/5 ml Guaiphenesin 100 mg/5 ml Sodium Citrate 200 mg/5 ml

A expektoranzien, kombinationen product containing methoxyphenamine hydrochloride + sodium citrate + guaiphenesin, registered in Ireland by Phoenix Labs Unlimited Company. The same ATC class is registered in 10 of our 19 countries.

ATC R05CA10

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedCasacol Expectorant SyrupMethoxyphena…ATCR05CA10REGISTER NO.IE-PA-PA1113/007/001PACKS LISTED1CHECKEDSeptember 28, 2026

Where it is registered

Expektoranzien, kombinationen is registered in 10 of 19 countries.

Countries holding a registration under ATC R05CA10 (expektoranzien, kombinationen), each read from that country’s own register.

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

Expektoranzien, kombinationen · ATC R05CA10

10 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Finlandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Spainprice
  • Switzerlandprice
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

HPRA (Ireland)
Active substance
Methoxyphenamine hydrochloride + Sodium citrate + Guaiphenesin
Manufacturer
Phoenix Labs Unlimited Company
Country
Ireland (IE)
ATC code
R05CA10
ATC class
Expektoranzien, Kombinationen
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    PA1113/007/001

Regulatory notes

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

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/7b49497c-a880-41d5-b3be-a661258cf55d
GET /v1/drugs/7b49497c-a880-41d5-b3be-a661258cf55d?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": "Syrup",
  "routes": [
    "Oral use"
  ],
  "source": "hpra",
  "atc_all": [
    "R05CA",
    "R05CA10"
  ],
  "strength": null,
  "pa_number": "PA1113/007/001",
  "substances": [
    "Methoxyphenamine hydrochloride",
    "Sodium citrate",
    "Guaiphenesin"
  ],
  "legal_basis": "Well-established use application (Article 10a of Directive No 2001/83/EC)",
  "market_info": "Marketed",
  "authorised_at": "23/05/1979",
  "dispensing_status": "Product not subject to medical prescription",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about expektoranzien, kombinationen.

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.