Germany· DE-A57-db60445ec8f41012
Ferro Aiwa
A medicinal product containing ferrous sulfate, registered in Germany by T&d Pharma Gmbh.
Checked against EMA Article 57 (European Union) on
Informational only — not a medical device.
The record
At a glance
EMA Article 57 (European Union)- Active substance
- Ferrous Sulfate
- Manufacturer
- T&d Pharma Gmbh
- Country
- Germany (DE)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- EMA Article 57 (European Union)
- Last checked
- September 30, 2026
Packs & prices · 0
No packs listed by the register for this record.
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.
- United StatesFerrous SulfateRichmond Pharmaceuticals Inc.
- BelgiumFero-Gradumet 525 mgTeofarma
- FranceFER AP-HP 0,5 mg NOUVEAU-NE, géluleASSISTANCE PUBLIQUE - HOPITAUX DE PARIS - AP-HP
- FinlandMicroferPfizer Health Ab
- NorwayDuroferonPerrigo Sverige AB
- ItalyFERRO-GRAD*40 cpr 105 mg rilascio prolungatoTEOFARMA Srl
Authorised across Europe · EMA
The same active substance is authorised in 12 EEA countries. Names it is sold under:
- Austria · Ferro - Gradumet
- Belgium · Fero-Gradumet
- 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 EMA Article 57 (European Union). 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/d5cc6efc-b233-4137-ad6c-14d0f13075ee GET /v1/drugs/d5cc6efc-b233-4137-ad6c-14d0f13075ee?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.
{
"pzn": null,
"route": "Oral Use",
"source": "ema_art57_de",
"ma_number": null,
"substance": "Ferrous Sulfate",
"atc_from_source": null,
"authorisation_country": "Germany"
}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.