United States· US:0220-1841_0a0ca58e-c4fc-ab5b-e063-6394a90ab630
Echinacea angustifolia
A echinacea angustifolia product containing echinacea angustifolia, registered in United States by Boiron. The same ATC class is registered in 2 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Echinacea angustifolia is registered in 2 of 19 countries.
Countries holding a registration under ATC L03AH02 (echinacea angustifolia), 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
Echinacea angustifolia · ATC L03AH02
2 / 19 countries
- Spainprice
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- ECHINACEA ANGUSTIFOLIA
- Manufacturer
- Boiron
- Country
- United States (US)
- ATC code
- L03AH02
- ATC class
- Echinacea angustifolia
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc1102201841416 [hp_C] in 1 TUBE (0220-1841-41)
- ndc110220-1841-41
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Echinacea angustifolia in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NetherlandsEchinacea angustifoliaHeel Belgium n.v.
- BelgiumEchinacea Angustifolia Boiron 200KBoiron
- SpainECHINAMED COMPRIMIDOSBioforce Espana A Vogel S.A.
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- Spain · Echinasor
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/abae7343-5809-44b1-8e73-70a04d16c49d GET /v1/drugs/abae7343-5809-44b1-8e73-70a04d16c49d?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": "6",
"substance": "ECHINACEA ANGUSTIFOLIA",
"productndc": "0220-1841",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[hp_C]/6[hp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about echinacea angustifolia.
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.