United States· US:37662-3699_029f57e7-2d6c-769c-e063-6294a90ab215
Zingiber Officinale
A medicinal product containing ginger, registered in United States by Hahnemann Laboratories, INC..
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
- GINGER
- 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
- ndc1137662-3699-1
- ndc1137662-3699-2
- ndc1137662-3699-3
- ndc1137662-3699-4
- ndc113766236991200 PELLET in 1 VIAL, GLASS (37662-3699-1)
- ndc113766236992500 PELLET in 1 VIAL, GLASS (37662-3699-2)
- ndc1137662369933000 PELLET in 1 BOTTLE, GLASS (37662-3699-3)
- ndc11376623699410000 PELLET in 1 BOTTLE, GLASS (37662-3699-4)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Ginger in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomBioCare Glucosamine MSM Complex tabletsBioCare Ltd
- SwitzerlandZintona, HartkapselnMIT Gesundheit Swiss GmbH
- GermanyIngwerwurzelstock (Pulver) GrünwalderGrünwalder Gesundheitsprodukte Gmbh
- PolandLokomotivaAflofarm Farmacja Polska Sp. z o.o.
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Austria · Tradimed Ingwer Rheuma
- Germany · Ingwerwurzelstock (Pulver) Grünwalder
- Netherlands · Tradimed
- Poland · Lokomotiva
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/e657a5cf-01ce-4f22-80ce-cb0667cd1368 GET /v1/drugs/e657a5cf-01ce-4f22-80ce-cb0667cd1368?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": "100",
"substance": "GINGER",
"productndc": "37662-3699",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about ginger.
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.