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United States· US:0121-1102_399b48d1-314a-4e14-9790-4cd22da7421c

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:0121-1102_399b48d1…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
    0121-1102-55

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/01f9fd19-7454-4c24-b207-1028c604c978
GET /v1/drugs/01f9fd19-7454-4c24-b207-1028c604c978?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": "RESPIRATORY (INHALATION)",
  "source": "ndc",
  "strength": "300",
  "substance": "PENTAMIDINE DIISETHIONATE",
  "productndc": "0121-1102",
  "dosage_form": "INHALANT",
  "dea_schedule": null,
  "strength_unit": "mg/300mg",
  "application_number": "ANDA206667",
  "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.