United States· US:55150-370_85e3dc1e-98ae-4c4c-8af9-237375475e08

VASOPRESSIN

A medicinal product containing vasopressin, registered in United States by Eugia US 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…normalisedVASOPRESSINATC—REGISTER NO.US:55150-370_85e3dc1e…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
VASOPRESSIN
Manufacturer
Eugia US 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
    55150-370-24
  • ndc11
    5515037024
    25 VIAL, MULTI-DOSE in 1 CARTON (55150-370-24) / 1 mL in 1 VIAL, MULTI-DOSE

Regulatory notes

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

Same medicine, other countries

Vasopressin in 13 other countries

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

All vasopressin products

Authorised across Europe · EMA

The same active substance is authorised in 27 EEA countries. Names it is sold under:

  • Austria · Empesin
  • Belgium · Reverpleg
  • Bulgaria · Емпресин
  • Czechia · Embesin
  • Germany · Argipressin Farmak, Empressin
  • Denmark · Empressin
  • Estonia · Empesin
  • Spain · Empressin
  • Finland · Empressin
  • France · Reverpleg
  • United Kingdom (Northern Ireland) · Argipressin Aop, Argipressin Mercury Pharmaceuticals
  • Greece · Empressin
  • Croatia · Empressin
  • Hungary · Embesyn
  • Ireland · Embesin
  • Italy · Empressin
  • Lithuania · Empesin
  • Luxembourg · Reverpleg
  • Latvia · Empesin
  • Netherlands · Empressine
  • Norway · Empressin
  • Poland · Argipressin Farmak, Empesin
  • Portugal · Empressin
  • Romania · Reverpleg
  • Sweden · Empressin
  • Slovenia · Empesin
  • Slovakia · Embesin

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/ce0f0b36-78b0-4706-923c-c86dce952ba2
GET /v1/drugs/ce0f0b36-78b0-4706-923c-c86dce952ba2?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": "INTRAVENOUS",
  "source": "ndc",
  "strength": "20",
  "substance": "VASOPRESSIN",
  "productndc": "55150-370",
  "dosage_form": "INJECTION",
  "dea_schedule": null,
  "strength_unit": "[USP'U]/mL",
  "application_number": "ANDA214314",
  "marketing_category": "ANDA"
}

See everything about vasopressin.

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.