United States· US:15631-2714_1a0ce0ba-fde9-5b55-e063-6294a90aec11
CUPRUM MET
A medicinal product containing copper, registered in United States by Rxhomeo Private Limited d.b.a. Rxhomeo, 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
- COPPER
- Manufacturer
- Rxhomeo Private Limited d.b.a. Rxhomeo, 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 · 4
- ndc11156312714010 mL in 1 BOTTLE (15631-2714-0)
- ndc11156312714130 mL in 1 BOTTLE (15631-2714-1)
- ndc1115631-2714-1
- ndc1115631-2714-0
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Copper in 7 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumAqua Cuprozincica Conforma 7.65 mg/ml - 25.5 mg/mlConforma
- United KingdomCopper gluconate 8mg tabletsBioCare Ltd
- NetherlandsCuprum metallicumHeel Belgium n.v.
- FinlandCUPRUM Alfaplex (Fu 1)
- FranceGRANIONS DE CUIVRE 0,3 mg/2 ml, suspension buvableGRANIONS
- IrelandCuprymina 925 MBq/mL radiopharmaceutical precursor, solutionA.C.O.M. Advanced Center Oncology Macerata S.r.l.
- CanadaMICRO CUSANDOZ CANADA INCORPORATED
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- France · Cuivre Granions, Oligosol
- Luxembourg · Cuivre Granions, Oligosol
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/ae556997-feeb-4d72-91aa-7377d90df8d1 GET /v1/drugs/ae556997-feeb-4d72-91aa-7377d90df8d1?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": "3",
"substance": "COPPER",
"productndc": "15631-2714",
"dosage_form": "LIQUID",
"dea_schedule": null,
"strength_unit": "[hp_X]/mL",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about copper.
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.