United States· US:0143-9514_a7e520ca-3213-4203-9a23-5295d82088e3

DROPERIDOL

A medicinal product containing droperidol, registered in United States by Hikma Pharmaceuticals USA Inc..

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedDROPERIDOLATC—REGISTER NO.US:0143-9514_a7e520ca…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DROPERIDOL
Manufacturer
Hikma Pharmaceuticals USA 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

  • ndc11
    0143951425
    25 VIAL in 1 CARTON (0143-9514-25) / 2 mL in 1 VIAL (0143-9514-01)
  • ndc11
    0143-9514-25

Regulatory notes

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

Same medicine, other countries

Droperidol in 12 other countries

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

All droperidol products

Authorised across Europe · EMA

The same active substance is authorised in 20 EEA countries. Names it is sold under:

  • Austria · Droperidol Aguettant, Droperidol Hikma
  • Belgium · Dehydrobenzperidol Substipharm, Droperidol Aguettant
  • Germany · Droperidol Aguettant, Droperidol Carinopharm
  • Denmark · Dehydrobenzperidol Substipharm, Droperidol Aguettant
  • Spain · Droperidol Hikma, Droperidol Kalceks
  • Finland · Dehydrobenzperidol Substipharm, Droperidol Aguettant
  • France · Droleptan, Droperidol Aguettant
  • United Kingdom (Northern Ireland) · Droperidol Hikma Farmacêutica (Portugal), Droperidol Panpharma
  • Greece · Xomolix
  • Hungary · Droperidol Kalceks
  • Ireland · Droperidol Aguettant, Droperidol Laboratoire Aguettant
  • Iceland · Dridol, Droperidol Aguettant
  • Italy · Droperidol Kalceks, Droperidolo Aguettant
  • Luxembourg · Dehydrobenzperidol Substiparm, Dehydrobenzperidol Substipharm
  • Latvia · Droperidol Kalceks
  • Netherlands · Dehydrobenzperidol Iv Substipharm, Dehydrobenzperidol Substipharm
  • Norway · Dridol, Droperidol Aguettant
  • Portugal · Droperidol Aguettant, Droperidol Hikma
  • Romania · Droperidol Aguettant
  • Sweden · Dridol, Droperidol Aguettant

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/d1e38439-72aa-4292-8774-aacbf5938842
GET /v1/drugs/d1e38439-72aa-4292-8774-aacbf5938842?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": "2.5",
  "substance": "DROPERIDOL",
  "productndc": "0143-9514",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "ANDA208197",
  "marketing_category": "ANDA"
}

See everything about droperidol.

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.