United States· US:0941-0681_348e030f-39eb-ac7c-e063-6394a90a4602

EXTRANEAL

A medicinal product containing icodextrin; sodium chloride; sodium lactate; calcium chloride; magnesium chloride, registered in United States by Vantive US Healthcare 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…normalisedEXTRANEALATC—REGISTER NO.US:0941-0681_348e030f…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
ICODEXTRIN; SODIUM CHLORIDE; SODIUM LACTATE; CALCIUM CHLORIDE; MAGNESIUM CHLORIDE
Manufacturer
Vantive US Healthcare 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
    0941068104
    4 BAG in 1 CARTON (0941-0681-04) / 2500 mL in 1 BAG (0941-0681-01)
  • ndc11
    0941-0681-04

Regulatory notes

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

Same medicine, other countries

Icodextrin; sodium chloride; sodium lactate; calcium chloride; magnesium chloride in 1 other country

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

All icodextrin; sodium chloride; sodium lactate; calcium chloride; magnesium chloride products

Authorised across Europe · EMA

The same active substance is authorised in 8 EEA countries. Names it is sold under:

  • Austria · Polithera
  • Czechia · Extraneal
  • Spain · Polithera
  • Italy · Icothera, Notecor
  • Netherlands · Polithera
  • Romania · Polithera
  • Sweden · Polithera
  • Slovakia · Extraneal Ikodextrín

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/fe05a976-11a6-4e25-942b-ca1b24023e3d
GET /v1/drugs/fe05a976-11a6-4e25-942b-ca1b24023e3d?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": "INTRAPERITONEAL",
  "source": "ndc",
  "strength": "7.5; 540; 450; 25.7; 5.1",
  "substance": "ICODEXTRIN; SODIUM CHLORIDE; SODIUM LACTATE; CALCIUM CHLORIDE; MAGNESIUM CHLORIDE",
  "productndc": "0941-0681",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "g/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE"
}

See everything about icodextrin; sodium chloride; sodium lactate; calcium chloride; magnesium chloride.

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.