Back to search

United States· US:0143-9210_a652f290-f8c6-4483-9fe4-b1fd50dec37d

Chloroprocaine Hydrochloride

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

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…normalisedChloroprocaine HydrochlorideATC—REGISTER NO.US:0143-9210_a652f290…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CHLOROPROCAINE HYDROCHLORIDE
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
    0143921010
    10 VIAL in 1 CARTON (0143-9210-10) / 20 mL in 1 VIAL (0143-9210-01)
  • ndc11
    0143-9210-10

Regulatory notes

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

Same medicine, other countries

Chloroprocaine hydrochloride in 12 other countries

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

All chloroprocaine hydrochloride products

Authorised across Europe · EMA

The same active substance is authorised in 22 EEA countries. Names it is sold under:

  • Austria · Ampres, Visiclor
  • Belgium · Ampres
  • Bulgaria · Ампрес
  • Germany · Ampres, Decelex
  • Denmark · Ampres
  • Estonia · Clorotekal
  • Spain · Ampres
  • Finland · Ampres
  • France · Clorotekal
  • United Kingdom (Northern Ireland) · Ampres
  • Greece · Ampres
  • Croatia · Clorotekal
  • Hungary · Clorotekal
  • Italy · Decelex
  • Luxembourg · Ampres
  • Latvia · Clorotekal
  • Netherlands · Ampres
  • Norway · Ampres
  • Poland · Ampres
  • Portugal · Ampres
  • Sweden · Ampres
  • Slovenia · Decelex

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/784a558e-4554-4b83-99b8-8227b2ee22f4
GET /v1/drugs/784a558e-4554-4b83-99b8-8227b2ee22f4?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": "EPIDURAL; INFILTRATION; INTRACAUDAL; PERINEURAL",
  "source": "ndc",
  "strength": "30",
  "substance": "CHLOROPROCAINE HYDROCHLORIDE",
  "productndc": "0143-9210",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "ANDA040273",
  "marketing_category": "ANDA"
}

See everything about chloroprocaine 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.