United States· US:84685-300_5d5134f8-4b97-4e65-a18a-654744214b53

LEROCHOL

A lerodalcibep product containing lerodalcibep, registered in United States by LIB Therapeutics, Inc.. The same ATC class is registered in 2 of our 19 countries.

ATC C10AX19

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedLEROCHOLATCC10AX19REGISTER NO.US:84685-300_5d5134f8…PACKS LISTED1CHECKEDSeptember 27, 2026

Where it is registered

Lerodalcibep is registered in 2 of 19 countries.

Countries holding a registration under ATC C10AX19 (lerodalcibep), each read from that country’s own register.

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

Lerodalcibep · ATC C10AX19

2 / 19 countries

  • Finlandprice
  • 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
LERODALCIBEP
Manufacturer
LIB Therapeutics, Inc.
Country
United States (US)
ATC code
C10AX19
ATC class
Lerodalcibep
Defined daily dose
4.5 g, O
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 1

  • ndc11
    84685-300-01

Regulatory notes

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

Same medicine, other countries

Lerodalcibep in 1 other country

What each register calls a product with the same active substance — salts and hydrates count as the same.

All lerodalcibep products

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/10ec237d-d8bc-44db-957a-bc12b6623282
GET /v1/drugs/10ec237d-d8bc-44db-957a-bc12b6623282?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": "SUBCUTANEOUS",
  "source": "ndc",
  "strength": "300",
  "substance": "LERODALCIBEP",
  "productndc": "84685-300",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/1.2mL",
  "application_number": "BLA761427",
  "marketing_category": "BLA"
}

See everything about lerodalcibep.

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.