United States· US:0002-7623_3af0bc84-13d6-46aa-a4c0-c62410b73bc6
Alimta
A medicinal product containing pemetrexed disodium heptahydrate, registered in United States by Eli Lilly and Company.
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 HEPTAHYDRATE
- Manufacturer
- Eli Lilly and Company
- 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
- ndc1100027623011 VIAL in 1 CARTON (0002-7623-01) / 20 mL in 1 VIAL
- ndc110002-7623-01
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Pemetrexed disodium heptahydrate in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- FinlandPemetrexed GlenmarkGlenmark Arzneimittel GmbH
- BelgiumPemetrexed Pharma D&S 100 mgPharmaceutical Development And Services
- IrelandPemetrexed Baxter 100 mg powder for concentrate for solution for infusionBaxter Holding B.V.
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- Spain · Pemetrexed Pharma D&s
- United Kingdom (Northern Ireland) · Pemetrexed Sun
- Italy · Pemetrexed Sun Pharma
- Netherlands · Pemetrexed Pharma D&s, Pemetrexed Sun
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/902958f8-0c10-4dfe-bb5e-41245acf243f GET /v1/drugs/902958f8-0c10-4dfe-bb5e-41245acf243f?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 HEPTAHYDRATE",
"productndc": "0002-7623",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/20mL",
"application_number": "NDA021462",
"marketing_category": "NDA"
}See everything about pemetrexed disodium heptahydrate.
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.