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United States· US:0517-2502_53245845-b446-46f8-bbe8-3323c58e10e5

Caffeine and Sodium Benzoate

A medicinal product containing caffeine, registered in United States by American Regent, 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…normalisedCaffeine and Sodium BenzoateATC—REGISTER NO.US:0517-2502_53245845…PACKS LISTED2CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
CAFFEINE
Manufacturer
American Regent, 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
    0517250210
    10 VIAL, SINGLE-DOSE in 1 BOX (0517-2502-10) / 2 mL in 1 VIAL, SINGLE-DOSE (0517-2502-01)
  • ndc11
    0517-2502-10

Regulatory notes

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

Same medicine, other countries

Caffeine in 12 other countries

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

All caffeine products

Authorised across Europe · EMA

The same active substance is authorised in 13 EEA countries. Names it is sold under:

  • Austria · Coffekapton
  • Belgium · Cafeine Sterop
  • Germany · Coffeinum N, Percoffedrinol N Aristo
  • Spain · Durvitan
  • France · Citrate De Cafeine Cooper, Percutafeine
  • United Kingdom (Northern Ireland) · Caffeine Citrate, Caffeine Citrate Brown & Burk Uk
  • Hungary · Coffeini Fono Viii. Naturland
  • Iceland · Gencebok, Peyona
  • Italy · Caffeina Citrato Monico
  • Liechtenstein · Gencebok, Peyona
  • Malta · Caffeine Citrate Monico
  • Norway · Gencebok, Peyona
  • Sweden · Koffein Viatris

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/278c00b8-aef7-42ef-a86f-634cf15392c9
GET /v1/drugs/278c00b8-aef7-42ef-a86f-634cf15392c9?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": "INTRAMUSCULAR; INTRAVENOUS",
  "source": "ndc",
  "strength": "125",
  "substance": "CAFFEINE",
  "productndc": "0517-2502",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED DRUG OTHER"
}

See everything about caffeine.

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.