United States· US:61314-044_d0e32882-06fe-4062-adae-3751ffc9979f
Trifluridine
A trifluridine product containing trifluridine, registered in United States by Sandoz Inc. The same ATC class is registered in 4 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Trifluridine is registered in 4 of 19 countries.
Countries holding a registration under ATC S01AD02 (trifluridine), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 3 of them publish a price we can compare per daily dose
Trifluridine · ATC S01AD02
4 / 19 countries
- Franceprice
- Norwayprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- TRIFLURIDINE
- Manufacturer
- Sandoz Inc
- Country
- United States (US)
- ATC code
- S01AD02
- ATC class
- Trifluridine
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1161314044751 BOTTLE, PLASTIC in 1 CARTON (61314-044-75) / 7.5 mL in 1 BOTTLE, PLASTIC
- ndc1161314-044-75
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Trifluridine in 5 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomTrifluridine 1% eye dropsSpecial Order
- BelgiumTrifluridine/Tipiracil Eugia 15 mg - 6.14 mgEugia Pharma (Malta)
- IrelandLonsurf 15 mg/6.14 mg film-coated tabletsLes Laboratoires Servier
- FranceVIROPHTA, préparation pour collyre (lyophilisat et solvant)HORUS PHARMA
- NorwayVirophtaHorus Pharma
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- France · Virophta
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 FDA National Drug Code directory (United States). 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/7cc02524-8539-447e-8ce0-7c1069718db8 GET /v1/drugs/7cc02524-8539-447e-8ce0-7c1069718db8?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.
{
"route": "OPHTHALMIC",
"source": "ndc",
"strength": "10",
"substance": "TRIFLURIDINE",
"productndc": "61314-044",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "ANDA074311",
"marketing_category": "ANDA"
}See everything about trifluridine.
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.