United States· US:64980-571_807ace4b-b2af-44b4-9371-884d73e21601

Methyldopa

A medicinal product containing methyldopa, registered in United States by Rising Pharma Holdings, Inc..

US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedMethyldopaATC—REGISTER NO.US:64980-571_807ace4b…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
METHYLDOPA
Manufacturer
Rising Pharma Holdings, Inc.
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

  • ndc11
    64980-571-01
  • ndc11
    6498057101
    100 TABLET in 1 BOTTLE (64980-571-01)

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 23 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
  • United Kingdom (Northern Ireland) · Methyldopa, Methyldopa Accord-Uk
  • 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 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/cfdb34c0-2e88-4e72-b06b-b3c5b1e98e37
GET /v1/drugs/cfdb34c0-2e88-4e72-b06b-b3c5b1e98e37?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": "250",
  "substance": "METHYLDOPA",
  "productndc": "64980-571",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "ANDA070076",
  "marketing_category": "ANDA"
}

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.