United States· US:83000-110_2c67a1db-151c-d067-e063-6394a90a5b06
GOHIBIC
A vilobelimab product containing vilobelimab, registered in United States by InflaRx GmbH. The same ATC class is registered in 8 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Vilobelimab is registered in 8 of 19 countries.
Countries holding a registration under ATC L04AJ10 (vilobelimab), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 5 of them publish a price we can compare per daily dose
Vilobelimab · ATC L04AJ10
8 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- VILOBELIMAB
- Manufacturer
- InflaRx GmbH
- Country
- United States (US)
- ATC code
- L04AJ10
- ATC class
- Vilobelimab
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1183000110044 VIAL, SINGLE-DOSE in 1 CARTON (83000-110-04) / 20 mL in 1 VIAL, SINGLE-DOSE
- ndc1183000-110-04
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Vilobelimab in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumGohibic 200 mgInflaRx
- CzechiaGOHIBICInflaRx GmbH, Jena
- FinlandGohibicInflaRx GmbH
- IrelandGohibic 200 mg Concentrate for solution for infusionInflaRx GmbH
- IcelandGohibicInflaRx GmbH
- NetherlandsGohibic 200 mg concentraat voor oplossing voor infusieInflaRx GmbH
- PolandGohibicInflaRx GmbH
- SwedenGohibic 200 mg Koncentrat till infusionsvätska, lösningInflaRx GmbH
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Gohibic
- Liechtenstein · Gohibic
- Norway · Gohibic
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/c430dbd4-574d-41ff-aa81-dd390d4db1db GET /v1/drugs/c430dbd4-574d-41ff-aa81-dd390d4db1db?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": "INTRAVENOUS",
"source": "ndc",
"strength": "10",
"substance": "VILOBELIMAB",
"productndc": "83000-110",
"dosage_form": "INJECTION",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": null,
"marketing_category": "EMERGENCY USE AUTHORIZATION"
}See everything about vilobelimab.
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.