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Ireland· IE-PA-PA22579/012/001

Dolutegravir Teva 50 mg film-coated tablets

A dolutegravir product containing dolutegravir sodium, registered in Ireland by TEVA GmbH. The same ATC class is registered in 13 of our 19 countries.

ATC J05AJ03

Checked against HPRA (Ireland) on

Informational only — not a medical device.

SOURCE REGISTER · IEHPRA (Ireland)normalisedDolutegravir Teva 50 mg film-coated t…ATCJ05AJ03REGISTER NO.IE-PA-PA22579/012/001PACKS LISTED1CHECKEDSeptember 28, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about dolutegravir sodiumAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Dolutegravir is registered in 13 of 19 countries.

Countries holding a registration under ATC J05AJ03 (dolutegravir), each read from that country’s own register.

  • This record: Ireland, from HPRA (Ireland)
  • 8 of them publish a price we can compare per daily dose
Search dolutegravir products by name

Dolutegravir · ATC J05AJ03

13 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • 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 dolutegravir costs, country by country.

Normalised to the WHO defined daily dose (50 mg), 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
Open the full comparison — free accountDrug prices for market access

Dolutegravir · price per daily dose (50 mg)

USD · FX 28 Sept 2026

  • CH Switzerland$25.85
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
Dolutegravir sodium
Manufacturer
TEVA GmbH
Country
Ireland (IE)
ATC code
J05AJ03
ATC class
Dolutegravir
Defined daily dose
50 mg, O
Reimbursed
Not published by this register
Source register
HPRA (Ireland)
Last checked
September 28, 2026

Packs & prices · 1

  • ie_pa_number
    PA22579/012/001

Regulatory notes

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

Interactions

94 interactions on record for dolutegravir.

Graded by severity as the source publishes them — 42 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
Check dolutegravir against other medicinesHow interaction checks work

Dolutegravir · interactions on record

94 records

  • 42 severe
  • 3 moderate
  • 49 minor

Most severe, free to view

  • Magnesium carbonateA02AA01severe
  • Magnesium oxideA02AA02severe
  • Magnesium hydroxideA02AA04severe
  • Kombinationen von AluminiumsalzenA02AB10severe
  • 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

Dolutegravir in 14 other countries

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

All dolutegravir products

Authorised across Europe · EMA

The same active substance is authorised in 5 EEA countries. Names it is sold under:

  • Cyprus · Dogrivio
  • Iceland · Tivicay
  • Liechtenstein · Tivicay
  • Norway · Dolutegravir Teva, Tivicay
  • Sweden · Dogrivio, Dolutegravir Elpen

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/1ab38ac9-2bcd-4522-a124-9e1d7af6d94f
GET /v1/drugs/1ab38ac9-2bcd-4522-a124-9e1d7af6d94f?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": [
    "J05AJ03"
  ],
  "strength": null,
  "pa_number": "PA22579/012/001",
  "substances": [
    "Dolutegravir sodium"
  ],
  "legal_basis": "Generic application (Article 10(1) of Directive No 2001/83/EC)",
  "market_info": "Not marketed",
  "authorised_at": "28/08/2026",
  "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 referenceMCP serverPlans

See everything about dolutegravir.

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.

Try it freeOpen in the console