United States· US:51662-1668_4ddcdfff-1469-bff0-e063-6294a90a5480
METHYLERGONOVINE MALEATE
A medicinal product containing methylergonovine maleate, registered in United States by HF Acquisition Co. LLC. DBA HealthFirst.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- METHYLERGONOVINE MALEATE
- Manufacturer
- HF Acquisition Co. LLC. DBA HealthFirst
- 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
- ndc1151662-1668-1
- ndc1151662166811 mL in 1 VIAL (51662-1668-1)
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Methylergonovine maleate in 11 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- GermanyMetherginEssential Pharma Limited
- NorwayMetherginNovartis
- SpainMETHERGIN 0,125 MG COMPRIMIDOS RECUBIERTOSEssential Pharma Limited
- ItalyMETHERGIN*15 cpr rivestite 0,125 mgESSENTIAL PHARMA (M) LTD
- FinlandMetherginNovartis Finland Oy
- IcelandMetherginEssential Pharma Limited
- CzechiaMETHYLERGOMETRIN PANPHARMA
- FranceMETHERGIN 0,20 mg/1 ml, solution injectable, ampouleESSENTIAL PHARMA (M) (MALTE)
Authorised across Europe · EMA
The same active substance is authorised in 12 EEA countries. Names it is sold under:
- Belgium · Methergin
- Bulgaria · Methergin, Метергин
- Germany · Methergin, Methergin®
- Denmark · Methergin
- Spain · Methergin, Methergín
- France · Methergin
- Greece · Demergin
- Iceland · Methergin
- Italy · Methergin
- Luxembourg · Methergin
- Netherlands · Methergin
- Sweden · Methergin
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/eb1dae3a-a6db-44ac-a231-1fd6fe6f5f5e GET /v1/drugs/eb1dae3a-a6db-44ac-a231-1fd6fe6f5f5e?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": "INTRAMUSCULAR; INTRAVENOUS",
"source": "ndc",
"strength": ".2",
"substance": "METHYLERGONOVINE MALEATE",
"productndc": "51662-1668",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": "ANDA090193",
"marketing_category": "ANDA"
}See everything about methylergonovine maleate.
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.