United States· US:49281-915_619c17f6-1c56-4821-9ce4-cfdd5d381d86

YF-VAX

A medicinal product containing yellow fever virus strain 17d-204 live antigen, registered in United States by Sanofi Vaccines US 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…normalisedYF-VAXATC—REGISTER NO.US:49281-915_619c17f6…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
YELLOW FEVER VIRUS STRAIN 17D-204 LIVE ANTIGEN
Manufacturer
Sanofi Vaccines US 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
    49281-915-01
  • ndc11
    49281-915-05

Regulatory notes

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

Same medicine, other countries

Yellow fever virus strain 17d-204 live antigen in 10 other countries

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

All yellow fever virus strain 17d-204 live antigen products

Authorised across Europe · EMA

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

  • Austria · Stamaril
  • Belgium · Stamaril
  • Bulgaria · Стамарил
  • Cyprus · Stamaril
  • Czechia · Stamaril
  • Germany · Stamaril
  • Denmark · Stamaril
  • Estonia · Stamaril
  • Spain · Stamaril
  • Finland · Stamaril
  • France · Stamaril
  • United Kingdom (Northern Ireland) · Stamaril
  • Hungary · Stamaril
  • Ireland · Stamaril
  • Iceland · Stamaril
  • Italy · Stamaril
  • Lithuania · Stamaril
  • Luxembourg · Stamaril
  • Latvia · Stamaril
  • Malta · Stamaril
  • Netherlands · Stamaril
  • Norway · Stamaril
  • Poland · Stamaril
  • Portugal · Stamaril
  • Romania · Stamaril
  • Sweden · Stamaril
  • Slovakia · Stamaril

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/17b6cee6-b4fc-478a-94c4-dd41f90fab6f
GET /v1/drugs/17b6cee6-b4fc-478a-94c4-dd41f90fab6f?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": "SUBCUTANEOUS",
  "source": "ndc",
  "strength": "4.74",
  "substance": "YELLOW FEVER VIRUS STRAIN 17D-204 LIVE ANTIGEN",
  "productndc": "49281-915",
  "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION",
  "dea_schedule": null,
  "strength_unit": "[PFU]/.5mL",
  "application_number": "BLA103915",
  "marketing_category": "BLA"
}

See everything about yellow fever virus strain 17d-204 live antigen.

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.