United States· US:55150-382_d9465d8d-67cb-4650-8c84-a9293d45ac92
Pemetrexed
A medicinal product containing pemetrexed disodium hemipentahydrate, registered in United States by Eugia US LLC.
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
- PEMETREXED DISODIUM HEMIPENTAHYDRATE
- Manufacturer
- Eugia US LLC
- 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
- ndc1155150382011 VIAL in 1 CARTON (55150-382-01) / 20 mL in 1 VIAL
- ndc1155150-382-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Pemetrexed disodium hemipentahydrate in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumCiambra 100 mgMenarini International Operations Luxembourg
- FinlandCiambraMenarini International Operations Luxembourg S.A.
- CzechiaARMISARTEActavis Group PTC ehf., Hafnarfjördur
- GermanyPemetrexed StadaStadapharm Gmbh
- IrelandPemetrexed Clonmel 25 mg/ml concentrate for solution for infusionClonmel Healthcare Ltd
- SwedenPemetrexed Zentiva 10 mg/ml Infusionsvätska, lösningZentiva k.s.
Authorised across Europe · EMA
The same active substance is authorised in 11 EEA countries. Names it is sold under:
- Austria · Pemetrexed Zentiva
- Germany · Pemetrexed Stada, Pemetrexed Zentiva
- Denmark · Pemetrexed Zentiva
- Spain · Pemetrexed Prasfarma
- Finland · Pemetrexed Zentiva
- France · Pemetrexed Zentiva
- United Kingdom (Northern Ireland) · Pemetrexed Zentiva
- Netherlands · Pemetrexed Zentiva
- Norway · Pemetrexed Zentiva
- Portugal · Pemetrexedo Stada
- Sweden · Pemetrexed Zentiva
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/fb9a3f2e-ac71-4803-871a-8060e35f7d2d GET /v1/drugs/fb9a3f2e-ac71-4803-871a-8060e35f7d2d?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": "INTRAVENOUS",
"source": "ndc",
"strength": "500",
"substance": "PEMETREXED DISODIUM HEMIPENTAHYDRATE",
"productndc": "55150-382",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/20mL",
"application_number": "ANDA214632",
"marketing_category": "ANDA"
}See everything about pemetrexed disodium hemipentahydrate.
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.