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United Kingdom· GB-APID-20325511000001101

Methyldopa 500mg tablets

A medicinal product containing methyldopa, registered in United Kingdom by Genesis Pharmaceuticals Ltd.

Checked against NHS dm+d (United Kingdom) on

Informational only — not a medical device.

SOURCE REGISTER · GBNHS dm+d (United Kingdom)normalisedMethyldopa 500mg tabletsATC—REGISTER NO.GB-APID-2032551100000…PACKS LISTED1CHECKEDSeptember 13, 2026

The record

At a glance

NHS dm+d (United Kingdom)
Active substance
Methyldopa
Manufacturer
Genesis Pharmaceuticals 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
    5060014441898

Regulatory notes

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

Same medicine, other countries

Methyldopa in 12 other countries

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

All methyldopa products

Authorised across Europe · EMA

The same active substance is authorised in 22 EEA countries. Names it is sold under:

  • Austria · Aldometil
  • Belgium · Aldomet
  • Bulgaria · Допегит
  • Cyprus · Dopamet, Methyldopa Remedica
  • Czechia · Dopegyt
  • Germany · Dopegyt, Methyldopa Stada
  • Denmark · Methyldopa Macure
  • Spain · Aldomet, Aldomet Forte
  • Finland · Methyldopa Macure
  • France · Aldomet
  • Hungary · Dopegyt
  • Italy · Aldomet
  • Lithuania · Dopegyt
  • Latvia · Dopegyt
  • Malta · Methyldopa Remedica
  • Netherlands · L-Methyldopa Teva, Methyldopa Cf
  • Norway · Methyldopa Macure
  • Poland · Dopegyt
  • Portugal · Aldomet, Aldomet Forte
  • Romania · Dopegyt
  • Sweden · Methyldopa Macure
  • Slovakia · Dopegyt

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/f9a0677a-0d46-4f18-bb35-4755a59c2f2a
GET /v1/drugs/f9a0677a-0d46-4f18-bb35-4755a59c2f2a?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": "20325511000001101",
  "desc": "Methyldopa 500mg tablets (Genesis Pharmaceuticals Ltd)",
  "form": "Oral tablet",
  "vpid": "42213411000001109",
  "source": "dmd",
  "vtm_id": "776747009",
  "strength": "500 mg",
  "substance": "Methyldopa",
  "ingredient": "Methyldopa (anhydrous)",
  "supplier_code": "20346911000001104"
}

See everything about methyldopa.

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.