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United States· US:87441-023_544eb617-ea1f-edf8-e063-6394a90afc72

Clonidine hydrochloride

A medicinal product containing clonidine hydrochloride, registered in United States by Unit Dose Solutions, 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…normalisedClonidine hydrochlorideATC—REGISTER NO.US:87441-023_544eb617…PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CLONIDINE HYDROCHLORIDE
Manufacturer
Unit Dose Solutions, 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 · 1

  • ndc11
    87441-023-01

Regulatory notes

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

Same medicine, other countries

Clonidine hydrochloride in 16 other countries

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

All clonidine hydrochloride products

Authorised across Europe · EMA

The same active substance is authorised in 23 EEA countries. Names it is sold under:

  • Austria · Catapresan
  • Belgium · Catapressan
  • Bulgaria · Хлофазолин
  • Czechia · Clonidine Olikla
  • Germany · Alcaridin, Catapresan
  • Denmark · Caruxin, Clopressan
  • Spain · Catapresan
  • Finland · Catapresan, Clonidine Macure
  • France · Catapressan
  • United Kingdom (Northern Ireland) · Calotep, Catapres
  • Greece · Catapresan
  • Ireland · Catapres, Catapres Ampoules
  • Italy · Catapresan, Catapresan Tts-1
  • Luxembourg · Catapressan
  • Latvia · Chlophazolin
  • Malta · Alcaridin, Catapres Tablets
  • Netherlands · Catapresan, Clonidine Hcl Cf
  • Norway · Caruxin, Clotaxip
  • Poland · Iporel
  • Portugal · Catapresan, Edolglau
  • Romania · Clonidină Arena, Clonidina Sintofarm
  • Sweden · Caruxin, Catapresan
  • Slovakia · Clonidine Olikla

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/c82e6b5a-1744-480b-9de5-9a9df756a062
GET /v1/drugs/c82e6b5a-1744-480b-9de5-9a9df756a062?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": "ORAL",
  "source": "ndc",
  "strength": ".1",
  "substance": "CLONIDINE HYDROCHLORIDE",
  "productndc": "87441-023",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "strength_unit": "mg/1",
  "application_number": "ANDA070923",
  "marketing_category": "ANDA"
}

See everything about clonidine hydrochloride.

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.