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United States· US:50742-539_149c50c5-59ad-4602-ad9e-58ad960eb91d

Dehydrated Alcohol

A medicinal product containing dehydrated alcohol, registered in United States by Ingenus Pharmaceuticals, LLC.

US label

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedDehydrated AlcoholATC—REGISTER NO.US:50742-539_149c50c5…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DEHYDRATED ALCOHOL
Manufacturer
Ingenus Pharmaceuticals, 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

  • ndc11
    5074253910
    10 VIAL, GLASS in 1 CARTON (50742-539-10) / 5 mL in 1 VIAL, GLASS (50742-539-01)
  • ndc11
    50742-539-10

Regulatory notes

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

Same medicine, other countries

Dehydrated alcohol in 9 other countries

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

All dehydrated alcohol products

Authorised across Europe · EMA

The same active substance is authorised in 10 EEA countries. Names it is sold under:

  • Belgium · Ethanol 96° Sterop
  • Bulgaria · Етилов Спирт, Етилов Спирт Bt
  • Germany · Ahd 2000, Alkohol-Konzentrat Braun
  • Spain · Alcohol Sanitario Reig Jofre
  • France · Alcool Modifie, Alcool Modifié Gifrer
  • Greece · Οινοπνευμα Mediplants, Οινοπνευμα Φαρμακευτικο Mediplants
  • Hungary · Alkohol Pharmamagist
  • Luxembourg · Alkohol-Konzentrat Braun, Sterillium Med
  • Poland · Desderman, Gargarisma Prophylacticum
  • Slovakia · Spiritus Concentratus Vulm, Spiritus Dilutus Vulm

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/bec83841-0a1b-49f4-bc3f-c974e8ef8e3e
GET /v1/drugs/bec83841-0a1b-49f4-bc3f-c974e8ef8e3e?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": "PERCUTANEOUS",
  "source": "ndc",
  "strength": "5",
  "substance": "DEHYDRATED ALCOHOL",
  "productndc": "50742-539",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mL/5mL",
  "application_number": "ANDA219569",
  "marketing_category": "ANDA"
}

See everything about dehydrated alcohol.

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.