United States· US:50881-006_4b5a0ce6-7f12-44aa-9b45-05188a37da9d

ZYNYZ

A retifanlimab product containing retifanlimab, registered in United States by Incyte Corporation. The same ATC class is registered in 10 of our 19 countries.

ATC L01FF10US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedZYNYZATCL01FF10REGISTER NO.US:50881-006_4b5a0ce6…PACKS LISTED2CHECKEDJuly 12, 2026

Where it is registered

Retifanlimab is registered in 10 of 19 countries.

Countries holding a registration under ATC L01FF10 (retifanlimab), each read from that country’s own register.

  • This record: United States, from FDA National Drug Code directory (United States)
  • 7 of them publish a price we can compare per daily dose

Retifanlimab · ATC L01FF10

10 / 19 countries

  • Belgiumprice
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Polandprice
  • Switzerlandprice
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
RETIFANLIMAB
Manufacturer
Incyte Corporation
Country
United States (US)
ATC code
L01FF10
ATC class
Retifanlimab
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
July 12, 2026

Packs & prices · 2

  • ndc11
    50881-006-03
  • ndc11
    5088100603
    1 VIAL, SINGLE-USE in 1 CARTON (50881-006-03) / 20 mL in 1 VIAL, SINGLE-USE

Regulatory notes

No shortage, Orange Book or US label notes for this record.

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/d1b6884f-9bbb-44c5-a3e2-564deee89d56
GET /v1/drugs/d1b6884f-9bbb-44c5-a3e2-564deee89d56?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": "25",
  "substance": "RETIFANLIMAB",
  "productndc": "50881-006",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "BLA761334",
  "marketing_category": "BLA"
}

See everything about retifanlimab.

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.