United States· US:68083-602_7c35e414-614e-4d70-96ff-3adae7238166
Travoprost Ophthalmic Solution
A travoprost product containing travoprost, registered in United States by Gland Pharma Limited. The same ATC class is registered in 18 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Travoprost is registered in 18 of 19 countries.
Countries holding a registration under ATC S01EE04 (travoprost), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 10 of them publish a price we can compare per daily dose
Travoprost · ATC S01EE04
18 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Franceprice
- Germany
- Icelandprice
- Ireland
- Italyprice
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Sweden
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- TRAVOPROST
- Manufacturer
- Gland Pharma Limited
- Country
- United States (US)
- ATC code
- S01EE04
- ATC class
- Travoprost
- Defined daily dose
- 0.1 ml, AT
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1168083602011 BOTTLE in 1 CARTON (68083-602-01) / 5 mL in 1 BOTTLE
- ndc1168083-602-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
70 interactions on record for travoprost.
Graded by severity as the source publishes them — 70 info. 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
Travoprost · interactions on record
70 records
Same medicine, other countries
Travoprost in 17 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaBONDULCTeva B.V., Haarlem
- NetherlandsLeachim 40 microgram/ml oogdruppels, oplossingAlfred E. Tiefenbacher GmbH & Co. KG
- FinlandBondulcActavis Group PTC ehf
- BelgiumDuoTrav 40 µg/ml - 5 mg/mlNovartis Europharm
- SwedenBondulc 40 mikrogram/ml Ögondroppar, lösningActavis Group PTC ehf.
- SwitzerlandTravatan, AugentropfenNovartis Pharma Schweiz AG
- IrelandTravatan 40 micrograms/mL eye drops, solutionNovartis Europharm Limited
- NorwayTravatanNovartis Europharm Limited (1)
Authorised across Europe · EMA
The same active substance is authorised in 28 EEA countries. Names it is sold under:
- Austria · Fredomat, Traglasin
- Belgium · Travoprost Eg, Vizitrav
- Bulgaria · Даверис, Травапрес
- Cyprus · Trav-Iop (Preservative Free), Travoprost Rafarm
- Czechia · Bondulc, Fredomat
- Germany · Fredomat, Travaprost Ratiopharm
- Denmark · Stavorio, Traglafka
- Estonia · Travoprost Elvim, Travoprost Zentiva
- Spain · Leachim, Sinetrav
- Finland · Travoprost Stada
- France · Sinetrav, Traglasin
- United Kingdom (Northern Ireland) · Travoprost Accord-Uk, Travoprost Aspire Pharma
- Greece · Stavorio, Trav-Iop
- Croatia · Vizitrav
- Iceland · Izba, Travatan
- Italy · Acamba, Brunitrav
- Liechtenstein · Izba, Travatan
- Lithuania · Traslor, Travoprost Elvim
- Luxembourg · Travoprost Eg, Vizitrav
- Latvia · Traslor, Travoprost Elvim
- Malta · Travic
- Netherlands · Leachim, Travapress
- Norway · Izba, Travatan
- Poland · Tipifree, Travoprost Genoptim
- Portugal · Travoprost Ciclum, Travoprost Rafarm
- Romania · Travapress, Travoprost Zentiva
- Sweden · Bondulc, Travoprost Medical Valley
- Slovakia · Travoprost 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 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/d4c8cae4-bf97-49ed-8661-149f8f8d6d10 GET /v1/drugs/d4c8cae4-bf97-49ed-8661-149f8f8d6d10?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": ".04",
"substance": "TRAVOPROST",
"productndc": "68083-602",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "ANDA218159",
"marketing_category": "ANDA"
}See everything about travoprost.
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.