United States· US:44911-0190_910b9b36-1958-47c7-9bdc-9615a69ea844
Glutathione
A glutathione product containing glutathione, registered in United States by Energique, Inc.. The same ATC class is registered in 4 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Glutathione is registered in 4 of 19 countries.
Countries holding a registration under ATC V03AB32 (glutathione), 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
Glutathione · ATC V03AB32
4 / 19 countries
- Japan
- Norwayprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- GLUTATHIONE
- Manufacturer
- Energique, Inc.
- Country
- United States (US)
- ATC code
- V03AB32
- ATC class
- Glutathione
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 1
- ndc1144911-0190-1
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Glutathione in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- NorwayRidutoxSoSe Pharma
- BelgiumViaspanBristol-Myers Squibb Belgium
- United KingdomSolgar L-Glutathione 50mg capsulesSolgar Vitamin and Herb
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- Italy · Gluthion, Hydroxia Esseti Farmaceutici
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/f4bf0f15-5578-4bfc-98a7-9df116870dd2 GET /v1/drugs/f4bf0f15-5578-4bfc-98a7-9df116870dd2?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": "5",
"substance": "GLUTATHIONE",
"productndc": "44911-0190",
"dosage_form": "LIQUID",
"dea_schedule": null,
"strength_unit": "[hp_X]/mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about glutathione.
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.