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United States· US:37662-0670_e1fa828f-be29-0fa0-e053-2a95a90a2f91

Echinacea Angustifolia

A medicinal product containing echinacea angustifolia whole, registered in United States by Hahnemann Laboratories, INC..

US 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…normalisedEchinacea AngustifoliaATC—REGISTER NO.US:37662-0670_e1fa828…PACKS LISTED8CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ECHINACEA ANGUSTIFOLIA WHOLE
Manufacturer
Hahnemann Laboratories, INC.
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 · 8

  • ndc11
    37662-0670-1
  • ndc11
    37662-0670-2
  • ndc11
    37662-0670-3
  • ndc11
    37662-0670-4
  • ndc11
    3766206701
    200 PELLET in 1 VIAL, GLASS (37662-0670-1)
  • ndc11
    3766206702
    500 PELLET in 1 VIAL, GLASS (37662-0670-2)
  • ndc11
    3766206703
    3000 PELLET in 1 BOTTLE, GLASS (37662-0670-3)
  • ndc11
    3766206704
    10000 PELLET in 1 BOTTLE, GLASS (37662-0670-4)

Regulatory notes

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

Same medicine, other countries

Echinacea angustifolia whole in 3 other countries

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

All echinacea angustifolia whole products

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/02d0b4e1-5af1-409c-b0ac-2400b8278bac
GET /v1/drugs/02d0b4e1-5af1-409c-b0ac-2400b8278bac?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": "500",
  "substance": "ECHINACEA ANGUSTIFOLIA WHOLE",
  "productndc": "37662-0670",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "strength_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about echinacea angustifolia whole.

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.