United States· US:37662-1252_e5d5eaf6-b5d3-b483-e053-2995a90af117
Selenium Metallicum
A medicinal product containing selenium, 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
- SELENIUM
- 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
- ndc1137662-1252-1
- ndc1137662-1252-2
- ndc1137662-1252-3
- ndc1137662-1252-4
- ndc113766212521200 PELLET in 1 VIAL, GLASS (37662-1252-1)
- ndc113766212522500 PELLET in 1 VIAL, GLASS (37662-1252-2)
- ndc1137662125233000 PELLET in 1 BOTTLE, GLASS (37662-1252-3)
- ndc11376621252410000 PELLET in 1 BOTTLE, GLASS (37662-1252-4)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Selenium in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United Kingdom200-SEL tabletsTriOn Pharma Ltd
- BelgiumSelenium Metallicum Boiron 15CHBoiron
- SwitzerlandSelenase peroral, TrinklösungPlavidente GmbH
- GermanyCefaselCefak Kg
- FinlandSelenium
- NorwaySelenoPrecisePharma Nord
- CanadaMICRO SESANDOZ CANADA INCORPORATED
Authorised across Europe · EMA
The same active substance is authorised in 6 EEA countries. Names it is sold under:
- Austria · Selenase
- Germany · Cefasel, Selenase
- Denmark · Selenoprecise, Selesyn
- France · Selenium Granions
- Italy · Selit
- Luxembourg · Selenium Granions
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/c10e1a85-ea59-4705-a594-d4032b9a8e82 GET /v1/drugs/c10e1a85-ea59-4705-a594-d4032b9a8e82?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": "SELENIUM",
"productndc": "37662-1252",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[hp_C]/1",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about selenium.
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.