Iceland· IS-EU/1/11/687/001-006 & 010-014
Hizentra
A humane immunglobuline, unspezifisch, extravaskulär product containing human normal immunoglobulin, registered in Iceland by CSL Behring GmbH*. The same ATC class is registered in 11 of our 19 countries.
Checked against Icelandic Medicines Agency (Iceland) on
Informational only — not a medical device.
Where it is registered
Humane immunglobuline, unspezifisch, extravaskulär is registered in 11 of 19 countries.
Countries holding a registration under ATC J06BA01 (humane immunglobuline, unspezifisch, extravaskulär), each read from that country’s own register.
- This record: Iceland, from Icelandic Medicines Agency (Iceland)
- 7 of them publish a price we can compare per daily dose
Humane immunglobuline, unspezifisch, extravaskulär · ATC J06BA01
11 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
The record
At a glance
Icelandic Medicines Agency (Iceland)- Active substance
- Human normal immunoglobulin
- Manufacturer
- CSL Behring GmbH*
- Country
- Iceland (IS)
- ATC code
- J06BA01
- ATC class
- Humane Immunglobuline, unspezifisch, extravaskulär
- Defined daily dose
- 1.4 g, P
- Reimbursed
- Not published by this register
- Source register
- Icelandic Medicines Agency (Iceland)
- Last checked
- September 29, 2026
Packs & prices · 7
7 priced- ean13963150 ml x1 hglISK 136155
- ean16731520 ml x1 hglISK 56408
- ean12524210 ml x1 áfsprISK 32500
- ean16070110 ml x1 hglISK 30398
- ean4268885 ml x1 hglISK 16338
- ean57246310 ml x10 hglISK 264042
- ean57505820 ml x1 áfsprISK 60613
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
48 interactions on record for humane immunglobuline, unspezifisch, extravaskulär.
Graded by severity as the source publishes them — 44 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
Humane immunglobuline, unspezifisch, extravaskulär · interactions on record
48 records
- 44 severe
- 4 minor
Most severe, free to view
- NeomycinA07AA01severe
- StreptomycinA07AA04severe
- Polymyxin BA07AA05severe
- Amphotericin BA07AA07severe
- 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
Humane immunglobuline, unspezifisch, extravaskulär in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumCuvitru 200 mg/mlBaxalta Innovations
- NorwayCuvitruBaxalta Innovations GmbH
- SwedenCuvitru 200 mg/ml Injektionsvätska, lösningBaxalta Innovations GmbH
- United StatesAlygloGC Biopharma Corp.
- SpainBERIGLOBINA PCsl Behring S.A.
- FinlandCutaquigOctapharma AB
- CzechiaGAMMANORMOctapharma (IP) SPRL, Brusel
- JapanｐＨ４処理酸性人免疫グロブリン（皮下注射）ＣＳＬベーリング
Authorised across Europe · EMA
The same active substance is authorised in 30 EEA countries. Names it is sold under:
- Austria · Cutaquig, Cuvitru
- Belgium · Cutaquig, Cuvitru
- Bulgaria · Имуновенин, Интратект
- Cyprus · Gamunex, Intratect
- Czechia · Cutaquig, Cuvitru
- Germany · Beriglobin, Cutaquig
- Denmark · Cutaquig, Cuvitru
- Estonia · Cutaquig, Gammanorm
- Spain · Cutaquig, Cuvitru
- Finland · Cutaquig, Cuvitru
- France · Clairyg, Cutaquig
- United Kingdom (Northern Ireland) · Cutaquig, Cuvitru
- Greece · Gaminex, Ig Vena
- Croatia · Cutaquig, Ig Vena
- Hungary · Cutaquig, Gammanorm
- Ireland · Cutaquig, Cuvitru
- Italy · Cutaquig, Cuvitru
- Liechtenstein · Deqsiga, Flebogamma Dif
- Lithuania · Cutaquig, Gammanorm
- Luxembourg · Cutaquig, Gammagard S/D (Solvent/Detergent)
- Latvia · Cutaquig, Gammanorm
- Malta · Cutaquig, Gammanorm
- Netherlands · Cutaquig, Cuvitru
- Norway · Cutaquig, Cuvitru
- Poland · Cutaquig, Cuvitru
- Portugal · Cutaquig, Gammanorm
- Romania · Cutaquig, Gammanorm
- Sweden · Cutaquig, Cuvitru
- Slovenia · Cutaquig, Gammanorm
- Slovakia · Cutaquig, Cuvitru
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/5bf1335e-ab0e-4c08-9e29-efebac7edbdb GET /v1/drugs/5bf1335e-ab0e-4c08-9e29-efebac7edbdb?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",
"source": "lyfjastofnun",
"atc_raw": "J06BA01",
"marketed": true,
"strength": "200 mg/ml",
"ma_number": "EU/1/11/687/001-006 & 010-014",
"substance": "Human normal immunoglobulin",
"other_info": "Ávísun lyfsins er bundin við sérfræðinga í ónæmisfræði, blóðsjúkdómum og krabbameinslækningum.",
"legal_status": "(R Z) Sérfræðingsmerkt (og lyfseðilsskylt)",
"ma_issued_serial": "40647"
}See everything about humane immunglobuline, unspezifisch, extravaskulär.
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.