United States· US:37662-3359_fe2381b8-413c-f3c3-e053-6294a90a53ab

Wheat Berry

A medicinal product containing wheat, registered in United States by Hahnemann Laboratories, INC..

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedWheat BerryATC—REGISTER NO.US:37662-3359_fe2381b…PACKS LISTED6CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
WHEAT
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 · 6

  • ndc11
    3766233591
    200 PELLET in 1 VIAL, GLASS (37662-3359-1)
  • ndc11
    3766233592
    1200 PELLET in 1 BOTTLE, GLASS (37662-3359-2)
  • ndc11
    3766233593
    4000 PELLET in 1 BOTTLE, GLASS (37662-3359-3)
  • ndc11
    37662-3359-1
  • ndc11
    37662-3359-2
  • ndc11
    37662-3359-3

Regulatory notes

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

Same medicine, other countries

Wheat in 2 other countries

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

All wheat products

Authorised across Europe · EMA

The same active substance is authorised in 2 EEA countries. Names it is sold under:

  • Germany · Prick-Testlösung Weizenmehl, Provokations-Testlösung Weizenmehl
  • Hungary · Alyostal Prick Növényi Eredetu Allergének Oldat Allergén Kivonatot Tartalmazó Oldatok, Allergiás Betegségek Diagnosztizálásában Használatos Prick Tesztek Végzésére, Staloral

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/e3e54c29-1b49-473b-bd9c-33ba2be2ab60
GET /v1/drugs/e3e54c29-1b49-473b-bd9c-33ba2be2ab60?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": "WHEAT",
  "productndc": "37662-3359",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "strength_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about wheat.

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.