United States· US:0220-2113_3a749d62-0e21-0c15-e063-6394a90ac1a8
FERRUM SULPHURICUM
A medicinal product containing ferrous sulfate, registered in United States by Boiron.
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
- FERROUS SULFATE
- Manufacturer
- Boiron
- 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 · 2
- ndc110220211341200 [kp_C] in 1 TUBE (0220-2113-41)
- ndc110220-2113-41
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Ferrous sulfate in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomActiFerr-S 200mg tabletsMaN Pharma Ltd
- PolandObsidanInPharm Sp. z o.o.
- BelgiumFero-Gradumet 525 mgTeofarma
- FranceFER AP-HP 0,5 mg NOUVEAU-NE, géluleASSISTANCE PUBLIQUE - HOPITAUX DE PARIS - AP-HP
- NorwayDuroferonPerrigo Sverige AB
- FinlandMicroferPfizer Health Ab
- GermanyEisensulfat LomapharmLomapharm Gmbh
- ItalyFERRO-GRAD*40 cpr 105 mg rilascio prolungatoTEOFARMA Srl
Authorised across Europe · EMA
The same active substance is authorised in 13 EEA countries. Names it is sold under:
- Austria · Ferro - Gradumet
- Belgium · Fero-Gradumet
- Germany · Eisensulfat Lomapharm, Ferro Aiwa
- Spain · Ferogradumet
- France · Fer Nouveau-Ne Ap-Hp
- United Kingdom (Northern Ireland) · Feospan, Ferrous Sulfate Wockhardt Uk
- Greece · Tardyferon
- Hungary · Ferro-Gradumet
- Lithuania · Tardyferon
- Luxembourg · Fero-Gradumet
- Norway · Duroferon, Ferromax
- Portugal · Ferro-Gradumet
- Slovakia · Tardyferon
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/3553d667-4473-45eb-bea2-f0b7ad34fad1 GET /v1/drugs/3553d667-4473-45eb-bea2-f0b7ad34fad1?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": "200",
"substance": "FERROUS SULFATE",
"productndc": "0220-2113",
"dosage_form": "PELLET",
"dea_schedule": null,
"strength_unit": "[kp_C]/200[kp_C]",
"application_number": null,
"marketing_category": "UNAPPROVED HOMEOPATHIC"
}See everything about ferrous sulfate.
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.