United States· US:0220-2366_f2f63f6f-bf2c-d47c-e053-2a95a90abf5b
Graphites
A medicinal product containing graphite, registered in United States by Boiron.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- GRAPHITE
- Manufacturer
- Boiron
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc110220236641200 [kp_C] in 1 TUBE (0220-2366-41)
- ndc110220-2366-41
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Graphite in 10 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumGraphites Boiron 15CHBoiron
- NetherlandsGraphitesHeel Belgium n.v.
- FinlandGraphites
- CzechiaPULFUNVUCyclomedica Ireland Limited, Dublin
- IrelandGRAPHITESA. Nelson & Company Limited
- SwitzerlandTetley Technegas, Generatormedeo AG
- IcelandPulmotecCyclomedica Ireland Limited
- GermanyPulmotecCyclomedica Ireland Limited
Authorised across Europe · EMA
The same active substance is authorised in 22 EEA countries. Names it is sold under:
- Austria · Pulmotec
- Belgium · Pulmotec
- Czechia · Pulfunvu
- Germany · Pulmotec
- Denmark · Pulmotec
- Spain · Pulmotec
- Finland · Pulmotec
- France · Pulmotec
- United Kingdom (Northern Ireland) · Pulmotec
- Greece · Pulmotec
- Croatia · Pulmotec
- Hungary · Pulmotec
- Ireland · Pulmotec
- Iceland · Pulmotec
- Italy · Pulmotec
- Luxembourg · Pulmotec
- Netherlands · Pulmotec
- Norway · Pulmotec
- Poland · Respiriscint
- Portugal · Pulmotec
- Sweden · Pulmotec
- Slovakia · Carbotech
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/b0f58cb0-27d0-4aa0-890f-ce3ef6febb8a GET /v1/drugs/b0f58cb0-27d0-4aa0-890f-ce3ef6febb8a?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": "ORAL",
"source": "ndc",
"strength": "200",
"substance": "GRAPHITE",
"productndc": "0220-2366",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[kp_C]/200[kp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about graphite.
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.