Sweden· SE-19840907000011
Lidokain-Fluorescein Bausch & Lomb 4 % + 0,25 % Ögondroppar, lösning i endosbehållare
A medicinal product containing fluorescein sodium + lidocaine hydrochloride, registered in Sweden by Bausch & Lomb Ireland Limited.
Checked against Swedish Medical Products Agency (Sweden) on
Informational only — not a medical device.
The record
At a glance
Swedish Medical Products Agency (Sweden)- Active substance
- Fluorescein Sodium + Lidocaine Hydrochloride
- Manufacturer
- Bausch & Lomb Ireland Limited
- Country
- Sweden (SE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- Swedish Medical Products Agency (Sweden)
- Last checked
- October 1, 2026
Packs & prices · 1
- se_varunummer19840907000011
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Fluorescein sodium + lidocaine hydrochloride in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SpainMINIMS LIDOCAINA/FLUORESCEINA 40 MG/ML + 2,5 MG/ML COLIRIO EN SOLUCION EN ENVASE UNIDOSISBausch + Lomb Ireland Limited
- United KingdomMinims lidocaine and fluorescein eye drops 0.5ml unit doseBausch & Lomb UK Ltd
- IrelandMinims Lidocaine Hydrochloride 4% w/v & Fluorescein Sodium 0.25% w/v Eye Drops, solutionBausch + Lomb Ireland Limited
- NetherlandsMinims Lidocaine-Fluoresceine, oogdruppels, oplossingBausch + Lomb Ireland Limited
Authorised across Europe · EMA
The same active substance is authorised in 8 EEA countries. Names it is sold under:
- Cyprus · Lidocaine & Fluorescein Bausch + Lomb
- Spain · Lidocaína/Fluoresceína Minims
- Greece · Lidocaine & Fluorescein Bausch + Lomb
- Hungary · Lidocaine/Fluorescein Health‐med
- Ireland · Minims
- Italy · Minims Diagnostico Con Anestetico
- Malta · Minims
- Netherlands · Minims
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 Swedish Medical Products Agency (Sweden). 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/5a8d0b32-196e-4803-b7bb-891215df2327 GET /v1/drugs/5a8d0b32-196e-4803-b7bb-891215df2327?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.
{
"source": "lakemedelsverket",
"doc_types": [
"SmPC",
"PL"
],
"se_npl_id": "19840907000011",
"product_page": "https://www.lakemedelsverket.se/sv/sok-lakemedelsfakta/lakemedel?id=19840907000011",
"product_doc_link": "https://docetp.mpa.se/LMF/Lidokain-Fluorescein%20Bausch%20%26%20Lomb%20eye%20drops%2C%20solution%20SmPC_09001bee807a5807.pdf"
}See everything about fluorescein sodium + lidocaine hydrochloride.
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.