United Kingdom· GB-APID-19805411000001107
Mydriasert 5.4mg/0.28mg ophthalmic inserts
A medicinal product containing phenylephrine + tropicamide, registered in United Kingdom by Thea Pharmaceuticals Ltd.
Checked against NHS dm+d (United Kingdom) on
Informational only — not a medical device.
The record
At a glance
NHS dm+d (United Kingdom)- Active substance
- Phenylephrine + Tropicamide
- Manufacturer
- Thea Pharmaceuticals Ltd
- Country
- United Kingdom (GB)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 2026
Packs & prices · 2
- gtin0793573718860
- gtin3662042000171
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Phenylephrine + tropicamide in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsMydriasert, ooginsert 0,28 mg en 5,4 mgLaboratoires Théa
- SwitzerlandMydriasert, insert ophtalmiqueTHEA Pharma S.A.
- SpainMYDRIASERT 0,28 mg/5,4 mg INSERTO OFTALMICOLaboratoires Thea
- FinlandMydriasertLaboratoires Thea
- FranceMYDRIASERT, insert ophtalmiqueTHEA
- NorwayMydriasertLaboratoires Théa
- SwedenMydriasert 0,28 mg/5,4 mg ÖgonlamellLaboratoires THEA
- GermanyMydriasertLaboratoires Thea
Authorised across Europe · EMA
The same active substance is authorised in 12 EEA countries. Names it is sold under:
- Austria · Mydriasert
- Belgium · Mydriasert
- Germany · Mydriasert
- Denmark · Mydriasert
- Spain · Mydriasert
- Finland · Mydriasert
- France · Mydriasert
- Italy · Mydriasert, Visumidriatic Fenilefrina
- Luxembourg · Mydriasert
- Netherlands · Mydriasert
- Portugal · Mydriasert
- Sweden · Mydriasert
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 NHS dm+d (United Kingdom). 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/68fe3374-f40e-47c2-83fe-010959011f71 GET /v1/drugs/68fe3374-f40e-47c2-83fe-010959011f71?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.
{
"apid": "19805411000001107",
"desc": "Mydriasert 5.4mg/0.28mg ophthalmic inserts (Thea Pharmaceuticals Ltd)",
"form": "Ophthalmic insert",
"vpid": "19805811000001109",
"source": "dmd",
"vtm_id": "19807811000001104",
"strength": "280 microgram",
"substance": "Phenylephrine + Tropicamide",
"ingredient": "Tropicamide",
"supplier_code": "14937811000001101"
}See everything about phenylephrine + tropicamide.
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.