Netherlands· NL-dc52ff58696f
Lumobry 0,25 mg/ml, oogdruppels, oplossing
A brimonidine product containing brimonidinetartraat, registered in Netherlands by Bausch + Lomb Ireland Limited. The same ATC class is registered in 7 of our 19 countries.
Checked against CBG-MEB (Netherlands) on
Informational only — not a medical device.
Where it is registered
Brimonidine is registered in 7 of 19 countries.
Countries holding a registration under ATC S01GA07 (brimonidine), each read from that country’s own register.
- This record: Netherlands, from CBG-MEB (Netherlands)
- 5 of them publish a price we can compare per daily dose
Brimonidine · ATC S01GA07
7 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Italyprice
- Netherlands
- Polandprice
The record
At a glance
CBG-MEB (Netherlands)- Active substance
- BRIMONIDINETARTRAAT
- Manufacturer
- Bausch + Lomb Ireland Limited
- Country
- Netherlands (NL)
- ATC code
- S01GA07
- ATC class
- Brimonidine
- Reimbursed
- Not published by this register
- Source register
- CBG-MEB (Netherlands)
- Last checked
- September 29, 2026
Packs & prices · 1
- cbg_meb_id127771
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
567 interactions on record for brimonidine.
Graded by severity as the source publishes them — 387 moderate. 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
Brimonidine · interactions on record
567 records
- 387 moderate
- 180 info
Most severe, free to view
- PapaverineA03AD01moderate
- MetoclopramideA03FA01moderate
- DimenhydrinatA04AB02moderate
- ThiethylperazinA04AB03moderate
- 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
Brimonidine in 17 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United StatesLUMIFY PRESERVATIVE FREE EYE DROPSBausch & Lomb Incorporated
- CzechiaLUMOBRYBAUSCH + LOMB IRELAND LIMITED, Dublin
- FinlandLumobryBausch + Lomb Ireland Limited
- FranceLUMOBRY 0,25 mg/mL, collyre en solutionLABORATOIRE CHAUVIN
- BelgiumLumobry 0.25 mg/mlBausch + Lomb Ireland
- PolandLumobryBausch+Lomb Ireland Ltd.
- SwedenLumobry 0,25 mg/ml Ögondroppar, lösningBausch + Lomb Ireland Limited
- IrelandLumobry 0.25 mg/mL eye drops, solutionBausch + Lomb Ireland Limited
Authorised across Europe · EMA
The same active substance is authorised in 29 EEA countries. Names it is sold under:
- Austria · Alpha-Vision Sine, Alphagan
- Belgium · Alphagan, Lumobry
- Bulgaria · Brimogen, Бримонидин Абр
- Cyprus · Brimontal, Corneax
- Czechia · Alphagan, Brimonidin Olikla
- Germany · Alphagan, Brimo-Vision
- Denmark · Alphagan, Brimonidintartrat 1a Farma
- Spain · Abradel, Alphagan
- Finland · Alphagan, Lumobry
- France · Alphagan, Brimazed
- United Kingdom (Northern Ireland) · Alphagan, Brimonidine Omnivision
- Greece · Alphagan, Brimofree
- Croatia · Alphagan, Bimanox
- Hungary · Brimogen, Lumobry
- Ireland · Alphagan, Lumobry
- Iceland · Alphagan, Brimonidin Bluefish
- Italy · Alphagan, Brimofree
- Liechtenstein · Mirvaso
- Lithuania · Brimonal, Brimonidine Tartrate Elvim
- Luxembourg · Alphagan, Brimonidin Micro Labs
- Latvia · Briglafre, Brimonal
- Malta · Alphagan, Brimogan
- Norway · Alphagan, Brymont
- Poland · Alphagan, Biprolast
- Portugal · Alphagan, Bglau
- Romania · Brimonal 2 Mg/Ml, Brimonidină Rompharm
- Sweden · Alphagan, Brimonidin Bluefish
- Slovenia · Bimanox, Luvify
- Slovakia · Brimonal, Brimonidin Olikla
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 CBG-MEB (Netherlands). 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/e1bc7b1a-96a7-4855-8cff-29017ad6a4d3 GET /v1/drugs/e1bc7b1a-96a7-4855-8cff-29017ad6a4d3?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": "Oogdruppels, oplossing",
"route": "Oculair gebruik",
"soort": "RVG",
"source": "cbg_meb",
"smpc_url": "https://www.geneesmiddeleninformatiebank.nl/smpc/h127771_smpc.pdf",
"strength": null,
"atc_label": "Brimonidine",
"detail_url": "https://www.geneesmiddeleninformatiebank.nl/nl/rvg127771",
"excipients": [
"BENZALKONIUMCHLORIDE",
"BOORZUUR (E 284)",
"BORAX 10-WATER (E 285)",
"CALCIUMCHLORIDE 2-WATER (E 509)",
"GLYCEROL (E 422)",
"KALIUMCHLORIDE (E 508)",
"NATRIUMCHLORIDE",
"NATRIUMHYDROXIDE (E 524)",
"WATER VOOR INJECTIE",
"ZOUTZUUR (E 507)"
],
"substances": [
"BRIMONIDINETARTRAAT"
],
"leaflet_url": "https://www.geneesmiddeleninformatiebank.nl/bijsluiters/h127771.pdf",
"authorised_at": "2022/09/08",
"procedure_number": "NL/H/5324/001",
"dispensing_status": "Uitsluitend recept",
"registration_number": "127771",
"additional_monitoring": "N"
}See everything about brimonidine.
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.