Back to search

United States· US:0121-1101_f1a6483e-a7cf-4b6e-9372-458a0a8982f9

Pentamidine Isethionate

A medicinal product containing pentamidine diisethionate, registered in United States by PAI Holdings, LLC dba PAI Pharma.

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedPentamidine IsethionateATC—REGISTER NO.US:0121-1101_f1a6483e…PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PENTAMIDINE DIISETHIONATE
Manufacturer
PAI Holdings, LLC dba PAI Pharma
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 · 1

  • ndc11
    0121-1101-02

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Pentamidine diisethionate in 8 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All pentamidine diisethionate products

Authorised across Europe · EMA

The same active substance is authorised in 13 EEA countries. Names it is sold under:

  • Belgium · Pentacarinat
  • Germany · Pentacarinat, Pentamidindiisetionat Tillomed
  • Denmark · Pentamidine Tillomed
  • Spain · Pentacarinat
  • Finland · Pentamidine Tillomed
  • France · Pentacarinat, Pentamidine Tillomed
  • United Kingdom (Northern Ireland) · Pentamidine Isetionate Tillomed
  • Ireland · Pentamidine Tillomed
  • Italy · Pentacarinat
  • Luxembourg · Pentacarinat
  • Netherlands · Pentacarinat, Pentamidinediisetionaat Tillomed
  • Norway · Pentamidine Diisetionate Tillomed
  • Sweden · Pentamidine Tillomed

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/1b8da8e9-b0e1-4b90-8b60-65d10d492a76
GET /v1/drugs/1b8da8e9-b0e1-4b90-8b60-65d10d492a76?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": "300",
  "substance": "PENTAMIDINE DIISETHIONATE",
  "productndc": "0121-1101",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/300mg",
  "application_number": "ANDA206666",
  "marketing_category": "ANDA"
}

See everything about pentamidine diisethionate.

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.