Iceland· IS-IS/1/16/034/01
Remurel
A glatiramer acetate product containing glatiramer acetat, registered in Iceland by Zentiva k.s.*. The same ATC class is registered in 14 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Glatiramer acetate is registered in 14 of 19 countries.
Countries holding a registration under ATC L03AX13 (glatiramer acetate), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 10 of them publish a price we can compare per daily dose
Glatiramer acetate · ATC L03AX13
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Icelandprice
- Ireland
- Italyprice
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Statesprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Glatiramer acetat
- Manufacturer
- Zentiva k.s.*
- Country
- Iceland (IS)
- ATC code
- L03AX13
- ATC class
- Glatiramer acetate
- Defined daily dose
- 20 mg, P
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 1
1 priced- ean02597828 áf.spr x1 pakkiISK 89920
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
2 interactions on record for glatiramer acetate.
Graded by severity as the source publishes them — 2 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
Glatiramer acetate · interactions on record
2 records
- 2 severe
Most severe, free to view
- NatalizumabL04AA23severe
- NatalizumabL04AG03severe
- 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.
Same medicine, other countries
Glatiramer acetate in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandCopaxone
- SpainCOPAXONE 20 mg/ml SOLUCION INYECTABLE EN JERINGA PRECARGADATeva Gmbh
- ItalyCOPAXONETEVA GMBH
- PolandCopaxoneTEVA GmbH
- NetherlandsBrabio 20 mg/ml, oplossing voor injectie in een voorgevulde spuitSynthon B.V.
- United KingdomBrabio 20mg/1ml solution for injection pre-filled syringesViatris UK Healthcare Ltd
- FranceCOPAXONE 20 mg/ml, solution injectable en seringue préremplieTEVA SANTE
- Japanグラチラマー酢酸塩T’sファーマ
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- France · Copaxone
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 Icelandic Medicines Agency (Iceland). 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/8f7c0d97-89bc-4b7a-a67b-5c6d13406efb GET /v1/drugs/8f7c0d97-89bc-4b7a-a67b-5c6d13406efb?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": "Stungulyf, lausn í áfylltri sprautu",
"source": "lyfjastofnun",
"atc_raw": "L03AX13",
"marketed": true,
"strength": "20 mg/ml",
"ma_number": "IS/1/16/034/01",
"substance": "Glatiramer acetat",
"other_info": "Ávísun lyfsins er bundin við sérfræðinga í taugasjúkdómum með sérþekkingu og reynslu í meðferð á MS.",
"legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
"ma_issued_serial": "42550"
}See everything about glatiramer acetate.
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.