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United States· US:42747-304_59579885-f5a8-41ba-bfc7-5e3adcc1cbce

CRYSVITA

A burosumab product containing burosumab, registered in United States by Kyowa Kirin, Inc.. The same ATC class is registered in 14 of our 19 countries.

ATC M05BX05US 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…normalisedCRYSVITAATCM05BX05REGISTER NO.US:42747-304_59579885…PACKS LISTED2CHECKEDJune 26, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about burosumabAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Burosumab is registered in 14 of 19 countries.

Countries holding a registration under ATC M05BX05 (burosumab), each read from that country’s own register.

  • This record: United States, from FDA National Drug Code directory (United States)
  • 9 of them publish a price we can compare per daily dose
Search burosumab products by name

Burosumab · ATC M05BX05

14 / 19 countries

  • Belgiumprice
  • Canada
  • Czechiaprice
  • Denmark
  • Finlandprice
  • Franceprice
  • Icelandprice
  • Ireland
  • Netherlands
  • Norwayprice
  • Polandprice
  • Switzerlandprice
  • United Kingdom
  • 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
BUROSUMAB
Manufacturer
Kyowa Kirin, Inc.
Country
United States (US)
ATC code
M05BX05
ATC class
Burosumab
Defined daily dose
2.5 mg, P
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
June 26, 2026

Packs & prices · 2

  • ndc11
    42747-304-01
  • ndc11
    4274730401
    1 mL in 1 VIAL, SINGLE-USE (42747-304-01)

Regulatory notes

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

Interactions

11 interactions on record for burosumab.

Graded by severity as the source publishes them — 9 severe. 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
Check burosumab against other medicinesHow interaction checks work

Burosumab · interactions on record

11 records

  • 9 severe
  • 2 moderate

Most severe, free to view

  • DihydrotachysterolA11CC02severe
  • CalcitriolA11CC04severe
  • CalcifediolA11CC06severe
  • ParicalcitolA11CC07severe
  • 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.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Burosumab in 15 other countries

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

All burosumab products

Authorised across Europe · EMA

The same active substance is authorised in 3 EEA countries. Names it is sold under:

  • Iceland · Crysvita
  • Liechtenstein · Crysvita
  • Norway · Crysvita

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/717b1939-0e4a-49c6-9123-ebb74b44c0f6
GET /v1/drugs/717b1939-0e4a-49c6-9123-ebb74b44c0f6?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": "30",
  "substance": "BUROSUMAB",
  "productndc": "42747-304",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "BLA761068",
  "marketing_category": "BLA"
}
API referenceMCP serverPlans

See everything about burosumab.

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.

Try it freeOpen in the console