United Kingdom· GB-APID-8993011000001107
InductOs 12mg powder and solvent and matrix for implantation matrix
A dibotermin alfa product containing dibotermin alfa, registered in United Kingdom by Medtronic Ltd. The same ATC class is registered in 11 of our 19 countries.
Checked against NHS dm+d (United Kingdom) on
Informational only — not a medical device.
Where it is registered
Dibotermin alfa is registered in 11 of 19 countries.
Countries holding a registration under ATC M05BC01 (dibotermin alfa), each read from that country’s own register.
- This record: United Kingdom, from NHS dm+d (United Kingdom)
- 7 of them publish a price we can compare per daily dose
Dibotermin alfa · ATC M05BC01
11 / 19 countries
- Belgiumprice
- Czechiaprice
- Denmark
- Finlandprice
- Icelandprice
- Ireland
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
The record
At a glance
NHS dm+d (United Kingdom)- Active substance
- Dibotermin alfa
- Manufacturer
- Medtronic Ltd
- Country
- United Kingdom (GB)
- ATC code
- M05BC01
- ATC class
- Dibotermin alfa
- Reimbursed
- Not published by this register
- Source register
- NHS dm+d (United Kingdom)
- Last checked
- September 13, 2026
Packs & prices · 2
- gtin00643169060081
- gtin00763000505608
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Dibotermin alfa in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CzechiaINDUCTOSMedtronic BioPharma B.V., Heerlen
- SwitzerlandInductOs 1.5 mg/ml, poudre 12 mg, solvant et matrice pour matrice pour implantationMedtronic BioPharma Sàrl
- FinlandInductosMedtronic BioPharma B. V.
- BelgiumInductOs 1.5 mg/mlMedtronic Biopharma
- IrelandInductOs 1.5 mg/ml powder, solvent and matrix for implantation matrixMedtronic BioPharma B.V.
- IcelandInductOsMedtronic BioPharma B.V.
- NorwayInductOsMedTronic BioPharma B.V.
- PolandInductOsMedtronic BioPharma B.V.
Authorised across Europe · EMA
The same active substance is authorised in 3 EEA countries. Names it is sold under:
- Iceland · Inductos
- Liechtenstein · Inductos
- Norway · Inductos
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 NHS dm+d (United Kingdom). 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/9816b57c-f942-4c67-9b50-e76de468b996 GET /v1/drugs/9816b57c-f942-4c67-9b50-e76de468b996?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.
{
"apid": "8993011000001107",
"desc": "InductOs 12mg powder and solvent and matrix for implantation matrix (Medtronic Ltd)",
"form": "Powder solvent and matrix for implantation matrix",
"vpid": "8992811000001109",
"source": "dmd",
"vtm_id": "775548005",
"strength": "12 mg",
"substance": "Dibotermin alfa",
"ingredient": "Dibotermin alfa",
"supplier_code": "19585811000001109"
}See everything about dibotermin alfa.
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.