United States· US:82584-700_4197af7c-fb98-684b-e063-6394a90a64cf
iVIZIA Dry Eye
A medicinal product containing povidone, registered in United States by Thea Pharma Inc..
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- POVIDONE
- Manufacturer
- Thea Pharma Inc.
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 6
- ndc1182584700051 BOTTLE, DROPPER in 1 CARTON (82584-700-05) / 5 mL in 1 BOTTLE, DROPPER
- ndc1182584700111 BOTTLE, DROPPER in 1 CARTON (82584-700-11) / 10 mL in 1 BOTTLE, DROPPER
- ndc1182584700131 BOTTLE, DROPPER in 1 CARTON (82584-700-13) / 5 mL in 1 BOTTLE, DROPPER
- ndc1182584-700-05
- ndc1182584-700-11
- ndc1182584-700-13
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Povidone in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FranceDULCILARMES 1,5 %, collyre en solutionHORUS PHARMA
- CzechiaARUFILBAUSCH + LOMB IRELAND LIMITED, Dublin
- BelgiumOculotect 50 mg/mlAlcon
- SwitzerlandProtagent SE, AugentropfenAlcon Switzerland SA
- United KingdomOculotect 5% eye drops 0.4ml unit doseAlcon Eye Care UK Ltd
- NetherlandsOculotect unidose 50 mg/ml, oogdruppelsEuro Registratie Collectief B.V.
- FinlandOculacAlcon Nordic A/S
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Belgium · Oculotect Unidose
- France · Dulcilarmes, Fluidabak
- Netherlands · Duratears Free, Oculotect
- Norway · Oculac
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/d8cd1fb6-a772-4361-a0bf-cd62fed65bbb GET /v1/drugs/d8cd1fb6-a772-4361-a0bf-cd62fed65bbb?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": "25",
"substance": "POVIDONE",
"productndc": "82584-700",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"strength_unit": "mg/5mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about povidone.
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.