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United Kingdom· GB-APID-4953011000001103

Tetanus immunoglobulin human 250unit solution for injection vials

A medicinal product containing tetanus immunoglobulin human, registered in United Kingdom by Bio Products Laboratory Ltd.

Checked against NHS dm+d (United Kingdom) on

Informational only — not a medical device.

SOURCE REGISTER · GBNHS dm+d (United Kingdom)normalisedTetanus immunoglobulin human 250unit …ATC—REGISTER NO.GB-APID-4953011000001…PACKS LISTED1CHECKEDSeptember 13, 2026

The record

At a glance

NHS dm+d (United Kingdom)
Active substance
Tetanus immunoglobulin human
Manufacturer
Bio Products Laboratory Ltd
Country
United Kingdom (GB)
ATC code
—
Reimbursed
Not published by this register
Source register
NHS dm+d (United Kingdom)
Last checked
September 13, 2026

Packs & prices · 1

  • gtin
    5019943000362

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Tetanus immunoglobulin human in 11 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All tetanus immunoglobulin human products

Authorised across Europe · EMA

The same active substance is authorised in 16 EEA countries. Names it is sold under:

  • Austria · Tetagam P
  • Belgium · Tetagam P
  • Czechia · Igantet
  • Germany · Tetagam P
  • Spain · Gamma Anti-Tétanos Grifols
  • France · Gammatetanos
  • Greece · Igantet, Tetagam P
  • Hungary · Tetagam P
  • Ireland · Tetagam P
  • Italy · Igantet, Tetanus Gamma
  • Malta · Tetagam P, Tetanus Gamma Kedrion
  • Netherlands · Tetagam P
  • Poland · Igantet
  • Portugal · Gamaglobulina Humana Antitetânica Pasteurizada Grifols, Tetagam P
  • Slovenia · Tetagam P
  • Slovakia · Igantet

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/eff98802-eef7-4c5f-b821-aa36d8395fad
GET /v1/drugs/eff98802-eef7-4c5f-b821-aa36d8395fad?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": "4953011000001103",
  "desc": "Tetanus immunoglobulin human 250unit solution for injection vials (Bio Products Laboratory Ltd)",
  "form": "Solution for injection",
  "vpid": "72171000001103",
  "source": "dmd",
  "vtm_id": "777724003",
  "strength": "250 unit",
  "substance": "Tetanus immunoglobulin human",
  "ingredient": "Tetanus immunoglobulin human",
  "supplier_code": "2065501000001104"
}

See everything about tetanus immunoglobulin human.

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.