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Ireland· IE-PA-EU/1/98/076/004

NovoNorm 0.5 mg tablets

A thiazolidinediones product containing repaglinide, registered in Ireland by Novo Nordisk A/S.

ATC A10BG

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedNovoNorm 0.5 mg tabletsATCA10BGREGISTER NO.IE-PA-EU/1/98/076/004PACKS LISTED1CHECKEDSeptember 28, 2026

The record

At a glance

HPRA (Ireland)
Active substance
Repaglinide
Manufacturer
Novo Nordisk A/S
Country
Ireland (IE)
ATC code
A10BG
ATC class
Thiazolidinediones
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    EU/1/98/076/004

Regulatory notes

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

Same medicine, other countries

Repaglinide in 17 other countries

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

All repaglinide products

Authorised across Europe · EMA

The same active substance is authorised in 24 EEA countries. Names it is sold under:

  • Austria · Repaglinid Ratiopharm, Repaglinid Sandoz
  • Belgium · Repaglinide Eg
  • Bulgaria · Индорин
  • Cyprus · Theroflan
  • Czechia · Vatinid
  • Germany · Repaglinid 1 A Pharma, Repaglinid Abz
  • Denmark · Repaglinid Doc Generici
  • Spain · Repaglinida Alter, Repaglinida Aurovitas
  • Finland · Repaglinid Stada
  • France · Repaglinide Arrow Lab, Repaglinide Biogaran
  • United Kingdom (Northern Ireland) · Repaglinide, Repaglinide Rivopharm Uk
  • Greece · Theroflan
  • Croatia · Reglinid, Repaglinid Pharmas
  • Iceland · Enyglid, Novonorm
  • Italy · Glicam, Repaglinide Aurobindo
  • Liechtenstein · Repaglinide Teva
  • Luxembourg · Repaglinide Eg
  • Latvia · Repaglinide Elvim
  • Malta · Repaglinide Aurobindo
  • Netherlands · Repaglinide Stada
  • Norway · Enyglid, Novonorm
  • Romania · Reneos, Repaglinida Arena
  • Sweden · Repaglinid Actavis, Repaglinid Stada
  • Slovenia · Repaglinid Stada

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/ff0c5e43-4279-44de-ad29-c4bc211a4524
GET /v1/drugs/ff0c5e43-4279-44de-ad29-c4bc211a4524?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": null,
  "source": "hpra",
  "atc_all": [
    "A10BG"
  ],
  "strength": null,
  "pa_number": "EU/1/98/076/004",
  "substances": [
    "Repaglinide"
  ],
  "legal_basis": "New active substance (Article 8(3) of Directive No 2001/83/EC)",
  "market_info": "Unknown",
  "authorised_at": "17/08/1998",
  "dispensing_status": "Product subject to prescription which may be renewed (B)",
  "registration_status": "AU",
  "supply_legal_status": "Supply through pharmacies only",
  "interchangeable_code": null
}

See everything about repaglinide.

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.