United States· US:71288-146_b369ac27-0118-4e53-be05-c9ba2dbf6875
Pemetrexed
A medicinal product containing pemetrexed disodium heptahydrate, registered in United States by Meitheal Pharmaceuticals Inc..
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
- Meitheal Pharmaceuticals 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
- ndc1171288146501 VIAL, SINGLE-DOSE in 1 CARTON (71288-146-50) / 20 mL in 1 VIAL, SINGLE-DOSE
- ndc1171288-146-50
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/ac2f632c-caf3-41c6-a48f-ea9c8a56ecb4 GET /v1/drugs/ac2f632c-caf3-41c6-a48f-ea9c8a56ecb4?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": "71288-146",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/20mL",
"application_number": "ANDA215479",
"marketing_category": "ANDA"
}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.