United States· US:0078-0743_4e6e6db9-e1cf-83cb-e063-6294a90a2420
ILEVRO
A nepafenac product containing nepafenac, registered in United States by Novartis Pharmaceuticals Corporation. The same ATC class is registered in 14 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Nepafenac is registered in 14 of 19 countries.
Countries holding a registration under ATC S01BC10 (nepafenac), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 8 of them publish a price we can compare per daily dose
Nepafenac · ATC S01BC10
14 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- NEPAFENAC
- Manufacturer
- Novartis Pharmaceuticals Corporation
- Country
- United States (US)
- ATC code
- S01BC10
- ATC class
- Nepafenac
- Defined daily dose
- 0.15 mg, AT
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 0
No packs listed by the register for this record.
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
81 interactions on record for nepafenac.
Graded by severity as the source publishes them — 81 moderate. 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
Nepafenac · interactions on record
81 records
- 81 moderate
Most severe, free to view
- DicoumarolB01AA01moderate
- WarfarinB01AA03moderate
- HeparinB01AB01moderate
- Antithrombin IIIB01AB02moderate
- Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Same medicine, other countries
Nepafenac in 13 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NorwayNevanacNovartis Europharm Limited (1)
- CzechiaNEVANACNovartis Europharm Limited, Dublin
- IrelandNevanac 3 mg/ml Eye drops, suspensionNovartis Europharm Limited
- IcelandNevanacNovartis Europharm Limited*
- NetherlandsNevanac 3 mg/ml oogdruppels, suspensieNovartis Europharm Limited
- PolandNevanacNovartis Europharm Limited
- SwedenNEVANAC 3 mg/ml Ögondroppar, suspensionNovartis Europharm Limited
- BelgiumNevanac 3 mg/mlNovartis Europharm
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Bulgaria · Апфекто
- Iceland · Nevanac
- Liechtenstein · Nevanac
- Norway · Nevanac
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/04e369fd-7bd3-49ef-aa28-e854de6faa28 GET /v1/drugs/04e369fd-7bd3-49ef-aa28-e854de6faa28?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": "3",
"substance": "NEPAFENAC",
"productndc": "0078-0743",
"dosage_form": "SUSPENSION/ DROPS",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "NDA203491",
"marketing_category": "NDA"
}See everything about nepafenac.
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.